Data / Medical devices / France / Peters Surgical
Peters Surgical: FDA-registered device maker in DOMALAIN Bretagne, France, 1 510(k) clearance
Peters Surgical is registered with the FDA (registration 3001650400) in DOMALAIN Bretagne, France. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated October 13, 1998. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3001650400
- Address
- Z.A. Vague De La Noe, DOMALAIN Bretagne, France, 35680
- Owner or operator
- PETERS SURGICAL (9009304)
- Roles
- Manufacturer, Specification developer
- First device listed
- June 8, 2016
- Registered through
- 2026
- Brand names listed
- Applier for VITALITEC Hemostatic Clips, CLIP 9 VITALITEC® TITANIUM HEMOSTATIC CLIP, GEM MicroClips, SLS-CLIP® VITALITEC TITANIUM HEMOSTATIC CLIP, VECTEC T'LIFT Laparoscopic retraction system
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applier, Hemostatic Clip | HBT | 1 | Specification developer | accessdata.fda.gov |
| Clip, Implantable | FZP | 2 | Manufacturer | accessdata.fda.gov |
| Laparoscopic Accessories, Gynecologic | NWV | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| October 13, 1998 | K981645 | TITANIUM HEMOSTATIC CLIP | FZP | Substantially Equivalent | Vitalitec Int'L., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Laparoscopic Accessories, Gynecologic
- All makers of Clip, Implantable
- All makers of Applier, Hemostatic Clip
Updated October 13, 1998. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.