Data / Medical devices / United States / Resilia Pharmaceuticals, Inc.
Resilia Pharmaceuticals, Inc.: FDA-registered device maker in Atlanta, GA, United States, 4 510(k) clearances
Resilia Pharmaceuticals, Inc. is registered with the FDA (registration 3030229896) in Atlanta, GA, United States. It lists 2 device types. The FDA files 4 510(k) clearances under its listings, the newest dated August 22, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3030229896
- Address
- 50 Glenlake Parkway Suite 450, Atlanta, GA, United States, 30328
- Owner or operator
- Resilia Pharmaceuticals, Inc. (10089572)
- Roles
- Specification developer
- First device listed
- December 19, 2023
- Registered through
- 2026
- Brand names listed
- Neocera Advanced Barrier Cream, Neosalus Cream, Neosalus Lotion, Recedo Topical Gel, Solace Cream
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | Specification developer | accessdata.fda.gov |
| Elastomer, Silicone, For Scar Management | MDA | 1 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 22, 2017 | K170911 | NEOCERA Advanced Barrier Cream | FRO | Substantially Equivalent | Exeltis USA Dermatology, LLC | accessdata.fda.gov |
| July 30, 2009 | K091719 | NEOSALUS LOTION | FRO | Substantially Equivalent | Quinnova Pharmaceuticals | accessdata.fda.gov |
| April 2, 2009 | K090585 | NEOSALUS CREAM | FRO | Substantially Equivalent | Quinnova Pharmaceuticals | accessdata.fda.gov |
| January 13, 2009 | K082089 | PRUMYX CREAM | FRO | Substantially Equivalent | Prugen, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 22, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.