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Sign in to claim this brandPETERS SURGICAL
US
Last updated May 27, 2026
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.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does Peters Surgical manufacture?
Peters Surgical specializes in surgical sutures and ligation devices. Their product range includes polyester sutures (both bioabsorbable and non-bioabsorbable, in monofilament and multifilament forms), nylon sutures (non-bioabsorbable, monofilament), and metallic sutures (monofilament). They also produce metallic ligation clips and open-surgery clip appliers. These devices are designed for use in various surgical procedures.
Where is Peters Surgical based, and what regulatory framework applies to their devices?
Peters Surgical is based in the United States. Their devices are regulated under the FDA’s Unique Device Identifier (UDI) system, which ensures traceability and compliance with U.S. medical device regulations. The company’s products are classified under FDA categories, including Class I and Class II, depending on their intended use and risk level.
Are Peters Surgical’s devices listed in any regulatory registries, and why does this matter?
Yes, Peters Surgical’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry is critical because it provides a standardized way to track and identify medical devices throughout their lifecycle, ensuring transparency, safety, and compliance with U.S. regulatory requirements. Listing in the UDI system helps healthcare providers, regulators, and manufacturers maintain accurate records.
How are Peters Surgical’s devices classified by regulatory authorities, and what does this classification mean?
Peters Surgical’s devices are classified as either Class I or Class II under FDA regulations. Classification determines the level of regulatory control and scrutiny a device undergoes. Class I devices generally pose the lowest risk and may require general controls, while Class II devices involve higher risks and require special controls to ensure safety and effectiveness. The classification ensures appropriate oversight based on the device’s potential impact on patient safety.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- —
- Website
- peters-surgical.com
- —
- —
- [email protected]
- Phone
- +1 508-747-6033
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 265741780
Catalogue (1040)
Page 4 of 21| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Corolene® | 20S20BF | FDA UDI | Class II | Active |
| Corolene® | 20N05G | FDA UDI | Class II | Active |
| Cardionyl® | 72106FH23 | FDA UDI | Class II | Active |
| Optime® | 18R40B | FDA UDI | Class II | Active |
| Corolene® | 20S35E | FDA UDI | Class II | Active |
| Optime® | 18S20V | FDA UDI | Class II | Active |
| Corolene® | 20S15JZ | FDA UDI | Class II | Active |
| Optime® | 18S35T | FDA UDI | Class II | Active |
| Corolene® | 20S10AH | FDA UDI | Class II | Active |
| Optime R | 12S20A | FDA UDI | Class II | Active |
| Cardioxyl ® | 73S30P | FDA UDI | Class II | Active |
| Optime® | 18G40F | FDA UDI | Class II | Active |
| Cardioxyl ® | 73P30AH | FDA UDI | Class II | Active |
| Optime® | 18N10C | FDA UDI | Class II | Active |
| Acier | 31805 | FDA UDI | Class II | Active |
| Optime® | 18I10E | FDA UDI | Class II | Active |
| Clip 9 Vitalitec | R9180 | FDA UDI | Class II | Active |
| Cardioxyl ® | 73S30AE | FDA UDI | Class II | Active |
| Applier, hemostatic clip | PB215-EB | FDA UDI | Class I | Active |
| Corolene® | 20S07G | FDA UDI | Class II | Active |
| Optime R | 12S35H | FDA UDI | Class II | Active |
| Corolene® | 20I15JZ | FDA UDI | Class II | Active |
| Corolene® | 20P05C | FDA UDI | Class II | Active |
| Cardionyl® | 72253 | FDA UDI | Class II | Active |
| Optime® | 18S07A | FDA UDI | Class II | Active |
| Corolene® | 20N07D | FDA UDI | Class II | Active |
| Optime® | 18S30M | FDA UDI | Class II | Active |
| Cardioxyl ® | 73S15P | FDA UDI | Class II | Active |
| Optime® | 18S35K | FDA UDI | Class II | Active |
| Advantime | 15S40C | FDA UDI | Class II | Active |
| Corolene® | 20S07F | FDA UDI | Class II | Active |
| Advantime | 15S35D | FDA UDI | Class II | Active |
| Corolene® | 20S15C | FDA UDI | Class II | Active |
| Cardionyl® | 720292 | FDA UDI | Class II | Active |
| Sinusorb® Pga | 8135 | FDA UDI | Class II | Active |
| Cardioxyl ® | 73P30P | FDA UDI | Class II | Active |
| Optime® | 18I20AA | FDA UDI | Class II | Active |
| Optime® | 18S50D | FDA UDI | Class II | Active |
| Optime® | 18I35AD | FDA UDI | Class II | Active |
| Optime® | 18I10G | FDA UDI | Class II | Active |
| Optime® | 18S10A | FDA UDI | Class II | Active |
| Corolene® | 20S20Y | FDA UDI | Class II | Active |
| Acier | 31804 | FDA UDI | Class II | Active |
| Sinusorb® Pga | 8139 | FDA UDI | Class II | Active |
| Corolene® | 20S07AJ | FDA UDI | Class II | Active |
| Optime® | 18RI35A | FDA UDI | Class II | Active |
| Cardioxyl ® | 73P30AN | FDA UDI | Class II | Active |
| Corolene® | 20S20AE | FDA UDI | Class II | Active |
| Clip 9 Vitalitec | R9324 | FDA UDI | Class II | Active |
| Optime® | 18S10K | FDA UDI | Class II | Active |
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Peters Surgical DOMALAIN Bretagne · FR FEI 3001650400