Data / Medical devices / United States / Curativa Bay LLC
Curativa Bay LLC: FDA-registered device maker in Largo, FL, United States, 1 510(k) clearance
Curativa Bay LLC is registered with the FDA (registration 3023994877) in Largo, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 2, 2025. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3023994877
- Address
- 2200 Tall Pines Dr Ste 104, Largo, FL, United States, 33771
- Owner or operator
- Curativa Bay LLC (10095751)
- Roles
- Repackager or relabeler
- First device listed
- April 23, 2026
- Registered through
- 2026
- Brand names listed
- Burn Care Spray, Wound Care Gel, Wound Care Spray
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | Repackager or relabeler | 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 |
|---|---|---|---|---|---|---|
| May 2, 2025 | K243457 | Nixall Antimicrobial Solutions Skin & Wound Hydrogel | FRO | Substantially Equivalent | Seriously Clean, Ltd. | accessdata.fda.gov |
Compare with other makers
Updated May 2, 2025. 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.