Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Boston ScientificLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Baylis Medical Technologies with 5 510(k) clearances. The most recent is a 510(k) clearance dated Jan 18, 2026: Baylis Connector Cable.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jan 18, 2026 | Baylis Connector CableK254114 · DSA | 510(k) clearances |
| Oct 28, 2025 | PrecisePath™ Radiofrequency Puncture Generator and PrecisePath™ FootswitchK250275 · GEI | 510(k) clearances |
| Sep 11, 2025 | PowerWire® 14 Radiofrequency Guidewire KitK251158 · PDU | 510(k) clearances |
| Feb 28, 2024 | PowerWire Radiofrequency Guidewire KitK232562 · PDU | 510(k) clearances |
| May 30, 2023 | RFP-100A Connector Cable (Single Use)K230571 · DSA | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
