Data / Medical devices / United States / Recibio, Inc.
Recibio, Inc.: FDA-registered device maker in Richmond, TX, United States, 1 510(k) clearance
Recibio, Inc. is registered with the FDA (registration 3015238043) in Richmond, TX, United States. It lists 5 device types. The FDA files 1 510(k) clearance under its listings, the newest dated January 26, 2015. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3015238043
- Address
- 1803 Rock Fence, Richmond, TX, United States, 77406
- Owner or operator
- Recibio, Inc. (10059285)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- December 18, 2018
- Registered through
- 2027
- Brand names listed
- CeaLogic - Ratio Applicator Kit, CeaLogic Amniotic Perforator, CeaLogic Specimen Collection Kit, Cealogic Film, Cealogic Ribbon
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Amniotome | HGE | 1 | Repackager or relabeler | accessdata.fda.gov |
| Syringe, Irrigating (Non Dental) | KYZ | 1 | Specification developer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 1 | Repackager or relabeler | accessdata.fda.gov |
| Trap, Sterile Specimen | BYZ | 2 | Manufacturer, Specification developer | accessdata.fda.gov |
| Wound Dressing With Animal-Derived Material(S) | KGN | 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 |
|---|---|---|---|---|---|---|
| January 26, 2015 | K143124 | KA01 Chitosan Wound Dressing | KGN | Substantially Equivalent | Foshan United Medical Technologies, Ltd. | accessdata.fda.gov |
Compare with other makers
- All makers of Amniotome
- All makers of Tape And Bandage, Adhesive
- All makers of Trap, Sterile Specimen
- All makers of Wound Dressing With Animal-Derived Material(S)
- All makers of Syringe, Irrigating (Non Dental)
Updated January 26, 2015. 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.