Peters Surgical
Country not established
Peters Surgical is a medical device manufacturer, with 1,226 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I) and 2 FDA recalls as of 12 Nov 2026.
- Devices
- 1,226
- FDA recalls
- 2
Registry facts
- Registries
- FDA GUDID 1,219
- EUDAMED 1,149
- FDA 510(k) 7
- Device classes
- FDA Class II 1,170
- FDA Class I 56
- FDA recalls
- Sites and related companies
- Peters Surgical France
- Identifiers
- DUNS 265741780
At a glance
Market reach
- United States
- FDA recalls
What Peters Surgical makes
Peters Surgical manufactures a range of surgical sutures, including polyester (both bioabsorbable and non-bioabsorbable), nylon, and metallic monofilament and multifilament variants, as well as bioabsorbable polyester sutures without antimicrobial properties. Their portfolio also includes metallic ligation clips and devices for applying these clips during open surgery.
The company’s products are regulated under the FDA’s UDI system, with devices classified as Class I and Class II. These sutures and clips are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device regulations.
Catalogue
Search and filter all 1,226 devicesShowing 1-50 of 1,226
Company details
- DUNS number
- 265741780
- Phone
- +1 508-747-6033
FDA recalls
FDA recall records list 2 recalls initiated by PETERS SURGICAL, initiated on 2014-06-25. By recorded status: 2 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2014
- 25 Jun 2014 Z-2675-2014 Class II Terminated A potential splitting of the surface treatment of the thread ends on certain sutures has recently been identified.
Full distribution text
- 25 Jun 2014 Z-2676-2014 Class II Terminated A potential splitting of the surface treatment of the thread ends on certain sutures has recently been identified.
Full distribution text
- 25 Jun 2014 Z-2675-2014 Class II Terminated A potential splitting of the surface treatment of the thread ends on certain sutures has recently been identified.
Sites
- Peters Surgical FRFEI 3004060107 0 devices
Frequently asked questions
How many devices does PETERS SURGICAL have in the registry?
The registry currently lists 1226 devices for PETERS SURGICAL. Devices recorded under merged duplicate company entries are counted once.
Which registries list PETERS SURGICAL's devices?
Among its 50 most recently registered devices, PETERS SURGICAL has devices listed in EUDAMED (50 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do PETERS SURGICAL's devices fall under?
Among its 50 most recently registered devices, the classes recorded for PETERS SURGICAL's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for PETERS SURGICAL?
FDA recall records list 2 recalls initiated by PETERS SURGICAL, the most recent initiated on 25 Jun 2014. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from PETERS SURGICAL in the registry?
The most recently registered devices listed for PETERS SURGICAL include OPTIME® 18S20P, OPTIME® 18S35AV, OPTIME® 18S30AW and COROLENE® 20S20U.