Company ยท US
Serpex Medical, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2022 to 2026. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (2 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 |
|---|---|---|---|
| Sep 2, 2026 | K262420 | Maverix Cryo Biopsy Pro (MCB Pro) (MCBP-1000); Maverix Cryo Cartridge (CC-1000) Serpex Medical | GEH |
| Jun 30, 2026 | K261068 | Maverix Cryo Biopsy Probe (MCB1000);Maverix Cryo Cartridge (CC1000) Serpex Medical | GEH |
| Oct 8, 2025 | K252874 | Compass Steerable Needle with Adapters SRA-1-01 and SRA-2-01 Serpex Medical, Inc. | KTI |
| Aug 25, 2022 | K221206 | Compass Steerable Needle Serpex Medical, Inc. | KTI |
| Aug 15, 2022 | K221302 | Recon Steerable Sheath Serpex Medical, Inc. | EOQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||