Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Baxter InternationalLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Synovis Life Technologies with 12 510(k) clearances. The most recent is a 510(k) clearance dated Apr 7, 2023: Peri-Guard and Supple Peri-Guard.
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.
| Apr 7, 2023 | Peri-Guard and Supple Peri-GuardK223052 · FTM | 510(k) clearances |
| Oct 19, 2022 | Vascu-Guard Vascular Repair PatchK221032 · PSQ | 510(k) clearances |
| Oct 19, 2022 | PERI-GUARD Repair Patch, SUPPLE PERI-GUARD Repair PatchK221029 · PSQ | 510(k) clearances |
| Oct 27, 2021 | PERI-STRIPS Dry Staple Line Reinforcement with VERITAS Collagen Matrix with SECURE GRIP TechnologyK213125 · FTM | 510(k) clearances |
| Dec 17, 2019 | Peri-Strips Dry with Veritas Collagen Matrix with Secure Grip Technology (PSDV-SG)K192615 · FTM | 510(k) clearances |
| Jan 16, 2015 | GEM Flow COUPLER Device and SystemK143589 · MVR | 510(k) clearances |
| Jan 7, 2015 | PERI-GUARD Repair Patch & SUPPLE PERI-GUARD Repair PatchK142447 · DXZ | 510(k) clearances |
| Nov 25, 2014 | VASCU-GUARD Peripheral Vascular PatchK142461 · DXZ | 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
