Data / Medical devices / United States / Advanced Bio-Technologies, Inc.
Advanced Bio-Technologies, Inc.: FDA-registered device maker in Tampa, FL, United States, 2 510(k) clearances
Advanced Bio-Technologies, Inc. is registered with the FDA (registration 3013057573) in Tampa, FL, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 14, 2006. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3013057573
- Address
- 4830 West Kennedy Blvd Suite 600, Tampa, FL, United States, 33609
- Owner or operator
- ADVANCED BIO-TECHNOLOGIES, INC. (10040429)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- April 12, 2012
- Registered through
- 2026
- Brand names listed
- BIOCORNEUM GEL, KELO-COTE SPRAY, KELOCOTE GEL; KELOCOTE UV; KELO COTE SOLAIRE
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Elastomer, Silicone, For Scar Management | MDA | 1 | Complaint file establishment, 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 |
|---|---|---|---|---|---|---|
| April 14, 2006 | K053481 | KELO-COTE SPRAY | MDA | Substantially Equivalent | Advanced Bio-Technologies, Inc. | accessdata.fda.gov |
| January 5, 2001 | K002488 | KELO-COTE TOPICAL GEL | MDA | Substantially Equivalent | Advanced Bio-Technologies, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 14, 2006. 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.