Company · NL
BAAT Medical Products B.V.
FDA 510(k) clearances and medical device recalls filed under this name, 2020 to 2026. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (3 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 22, 2026 | K262184 | GANNET® BAAT Medical Products B.V., NL | JDO |
| Mar 16, 2026 | K254176 | SINEFIX BAAT Medical Products B.V., NL | MBI |
| Jan 15, 2026 | K251961 | SDS Growing Rod BAAT Medical Products B.V., NL | PGM |
| Mar 8, 2023 | K220966 | SINEFIX BAAT Medical Products B.V., NL | MBI |
| Sep 14, 2021 | K211474 | Kleiner KG2 System BAAT Medical Products B.V., NL | MAX |
| Aug 27, 2020 | K201830 | ANSER Clavicle Pin BAAT Medical Products B.V., NL | HSB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||