EXHIBIT 99.1

Appendix 4C

Quarter Ended 31 December 2015

San Diego, California and Sydney, Australia (Friday, 29 January 2016, AEDT) – REVA Medical, Inc. (ASX: RVA) (“REVA” or the “Company”) is pleased to provide the attached Appendix 4C Quarterly Report for the quarter ended 31 December 2015. The Appendix 4C is unaudited.

Fourth Quarter Highlights

During the fourth quarter of 2015, the Company’s operating activities continued to focus on the clinical study of its Fantom scaffold. In addition to announcing the enrollment of 110 patients on 30 September 2015, the Company also presented preliminary clinical data on Fantom at the Transcatheter Cardiovascular Therapeutics (“TCT”) conference in October, which was being held in San Francisco. Fantom is a bioresorbable drug-eluting scaffold that utilizes REVA’s advanced proprietary polymer to allow thinner strut thickness and enhanced deliverability, while offering its unique property of being visible under x-ray.

The enrollment of the first 110 patients in the FANTOM II trial marked a milestone for the Company in its goal to commercialize Fantom. These patients will undergo an imaging assessment at six months; this data is planned to be collected in the second quarter and used in a CE Mark application in the third quarter of this year. If approved, the CE Mark would allow REVA to sell in Europe and other countries that recognize the CE Mark. In addition to this first set of patients, the Company began enrolling a second set of 110 patients during the fourth quarter of 2015, with completion of enrollment expected early in the second quarter of this year, for total enrollment of at least 220 patients. Data from this second set of patients will be used for market support and other commercial purposes.

The clinical data presented at the TCT conference included the complete data set from the FANTOM I study of seven patients; this data showed perfect procedural success and very good safety results with no major adverse cardiac events (“MACE”) through six months. The interim data presented on FANTOM II also showed very good procedural success and low MACE rates for the limited data available. Both sets of study results confirmed sustained restoration of blood flow. Subsequent to the end of the fourth quarter, at the J.P. Morgan Healthcare conference in January 2016, the Company presented updated data on both Fantom clinical studies. The updated data showed continued safety with low MACE rates. The next planned release of clinical data will be at the Paris Course on Revascularization in May.

In addition to the clinical progress during the fourth quarter, the Company’s technical team continued producing scaffolds to support clinical enrollments and continued testing and assembling processes work to support the scale-up of manufacturing for commercialization. As announced earlier this month and supporting the goal of commercialization, the Company hired Mr. Richard Kimes as Sr. Vice President of Operations. Mr. Kimes has over 25 years of experience in the medical device industry with companies that include Volcano Corporation, Guidant Corporation, Elixir Medical Corporation, and mNemoscience GmbH.

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HEAD OFFICE:  5751 Copley Drive, San Diego, CA 92111   •   +1 (858) 966-3000   •   +1 (858) 966-3099 (FAX)   •   www.revamedical.com

AUSTRALIAN OFFICE: Suite 4, Level 14, 6 O’Connell Street, Sydney NSW 2000   •   +61 2 9237 2800

ARBN 146 505 777   •   REVA Medical, Inc., is a foreign company incorporated in Delaware, USA, whose stockholders have limited liability

REVA Medical, Inc. – ASX AnnouncementPage 2

Early in the fourth quarter, on 1 October 2015, the Company announced receipt of US$9,506,000 cash proceeds from the issuance of 4,375,000 shares of common stock upon the exercise of warrants. The warrants had been issued under the convertible note financing on 14 November 2014. Following this exercise, a total of 4,375,000 warrants remain outstanding with an exercise value of US$11,407,000; the Company is currently pursuing exercise of these remaining warrants.

Appendix 4C

As of 31 December 2015, the Company’s cash balance was US$16,895,000. The current quarter end cash balance reflects an increase of US$5,050,000 from the 30 September 2015 quarter end balance of US$11,845,000. This increase reflects the receipt of US$9,506,000 in warrant exercise proceeds, US$347,000 in employee plan option exercise proceeds, and US$497,000 from maturing certificates of deposit investment. These receipts were offset by US$5,205,000 in disbursements related to normal operating activities and capital equipment purchases of US$95,000.

The Company currently plans to lodge its Appendix 4E Preliminary Final Report with the Australian Securities Exchange on or before the due date of 29 February 2016 and file its Form 10-K Annual Report, including audited financial statements, with the U.S. Securities and Exchange Commission on or before the due date of 15 March 2016.

About REVA

REVA is a clinical stage medical device company located in San Diego, California, USA, that is working to commercialize its proprietary bioresorbable stents, which are called “scaffolds” because of their temporary nature. The Company’s scaffolds have been developed as an alternative to metal stents, which are small tube-like devices permanently implanted into an artery to treat coronary artery disease. Scaffolds provide restoration of blood flow, support the artery through the healing process, then disappear (or “resorb”) from the body over a period of time. This resorption allows the return of natural movement and function of the artery, a result not attainable with permanent metal stents. The Company’s initial product, the Fantom® scaffold, has been designed to offer an ideal balance of thinness and strength and distinct ease-of-use features including complete scaffold visibility under x-ray, expansion with one continuous inflation, and no procedural time limitations. REVA will require successful clinical trial results and regulatory approval before it can commercialize Fantom or any other products.

Forward-Looking Statements

This announcement contains or may contain forward-looking statements that are based on management's beliefs, assumptions and expectations and on information currently available to management. All statements that are not statements of historical fact, including those statements that address future operating performance and events or developments that we expect or anticipate will occur in the future, are forward-looking statements, such as those statements regarding our ability to obtain regulatory approvals, timely and successfully complete our clinical trials, protect our intellectual property position, commercialize our products if and when approved, develop and commercialize new products, recruit and retain our key personnel, and estimates regarding our capital requirements and financial performance. You should not place undue reliance on forward-looking statements. Although management believes forward-looking statements are reasonable as and when made, forward-looking statements are subject to a number of risks and uncertainties that may cause our actual results to vary materially from those expressed in forward-looking statements, including the risks and uncertainties that are described in the "Risk Factors" section of our Annual Report on Form 10-K filed with the US Securities and Exchange Commission (the “SEC”) on March 30, 2015, and as may be updated in our periodic reports thereafter. Any forward-looking statements in this announcement speak only as of the date when made. REVA does not assume any obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events, or otherwise.

__________________________________________________________________________________________

HEAD OFFICE:  5751 Copley Drive, San Diego, CA 92111   •   +1 (858) 966-3000   •   +1 (858) 966-3099 (FAX)   •   www.revamedical.com

AUSTRALIAN OFFICE: Suite 4, Level 14, 6 O’Connell Street, Sydney NSW 2000   •   +61 2 9237 2800

ARBN 146 505 777   •   REVA Medical, Inc., is a foreign company incorporated in Delaware, USA, whose stockholders have limited liability

Appendix 4C

Quarterly report for entities

admitted on the basis of commitments

Rule 4.7B

Appendix 4C

Quarterly report

for entities admitted

on the basis of commitments

Introduced 31/03/00  Amended 30/09/01, 24/10/05, 17/12/10

Consolidated statement of cash flows

+ See chapter 19 for defined terms.

17/12/2010Appendix 4C Page 1

Appendix 4C

Quarterly report for entities

admitted on the basis of commitments

+ See chapter 19 for defined terms.

Appendix 4C

Quarterly report for entities

admitted on the basis of commitments

Payments to directors of the entity and associates of the directors

Payments to related entities of the entity and associates of the related entities

Non-cash financing and investing activities

Financing facilities available

Add notes as necessary for an understanding of the position.

+ See chapter 19 for defined terms.

Appendix 4C

Quarterly report for entities

admitted on the basis of commitments

Reconciliation of cash

Acquisitions and disposals of business entities

Compliance statement

(Chief Financial Officer/Company Secretary)

Print name:  Katrina L. Thompson

+ See chapter 19 for defined terms.

Appendix 4C

Quarterly report for entities

admitted on the basis of commitments

Notes

+ See chapter 19 for defined terms.