Company · CA
Baylis Medical Technologies, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2023 to 2026. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (1 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 |
|---|---|---|---|
| Jan 18, 2026 | K254114 | Baylis Connector Cable Baylis Medical Technologies, Inc., CA | DSA |
| Oct 28, 2025 | K250275 | PrecisePath Radiofrequency Puncture Generator and PrecisePath Footswitch Baylis Medical Technologies, Inc., CA | GEI |
| Sep 11, 2025 | K251158 | PowerWire® 14 Radiofrequency Guidewire Kit Baylis Medical Technologies, Inc., CA | PDU |
| Feb 28, 2024 | K232562 | PowerWire Radiofrequency Guidewire Kit Baylis Medical Technologies, Inc., CA | PDU |
| May 30, 2023 | K230571 | RFP-100A Connector Cable (Single Use) Baylis Medical Technologies, Inc., CA | DSA |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||