Is this your brand? Sign in to claim ownership.
Sign in to claim this brandCp Medical
US
Last updated May 23, 2026
Information
- Country
- US
- Address
- —
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (435)
Page 8 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| C-Ptfe | 600E | FDA UDI | Class II | Active |
| Polybond | CP1066A | FDA UDI | Class II | Active |
| Visorb | 468A | FDA UDI | Class II | Active |
| Monoswift | L497 | FDA UDI | Class II | Active |
| Cp Fiber | ST649 | FDA UDI | Class II | Active |
| Plain Gut | 822PG-IMC | FDA UDI | Class II | Active |
| Polypro | 8665P | FDA UDI | Class II | Active |
| Polypro | 8690P | FDA UDI | Class II | Active |
| Monoswift | L310 | FDA UDI | Class II | Active |
| Visorb | 364A | FDA UDI | Class II | Active |
| Monomid | 690B | FDA UDI | Class II | Active |
| Nylon | MS-40B | FDA UDI | Class II | Active |
| Polypro | 8634P | FDA UDI | Class II | Active |
| Visorb | U385A | FDA UDI | Class II | Active |
| Cp Fiber | CPF-40-18-DA | FDA UDI | Class II | Active |
| Monomid | 945B | FDA UDI | Class II | Active |
| Polybond | CP683A | FDA UDI | Class II | Active |
| Polypropylene | 8682P-IMC | FDA UDI | Class II | Active |
| Chromic Gut | 636CG-IMC | FDA UDI | Class II | Active |
| Visorb Quick | VQ490 | FDA UDI | Class II | Active |
| Monomid | 661B | FDA UDI | Class II | Active |
| Visorb | 603A | FDA UDI | Class II | Active |
| Fn Needles | FN17-51T | FDA UDI | Class II | Active |
| Visorb | 340A | FDA UDI | Class II | Active |
| Polybond | CP563A | FDA UDI | Class II | Active |
| Polyester | ECN-E12048L | FDA UDI | Class II | Active |
| Cp Fiber | CPF-02K | FDA UDI | Class II | Active |
| Monomid | 664B | FDA UDI | Class II | Active |
| Polybond | CP588A | FDA UDI | Class II | Active |
| Mono-Dox | M195 | FDA UDI | Class II | Active |
| Polybond | CP1021A | FDA UDI | Class II | Active |
| C-Ptfe | 202ERT | FDA UDI | Class II | Active |
| Polybond | CP833A | FDA UDI | Class II | Active |
| Polypro | 8524P | FDA UDI | Class II | Active |
| Polypro | 9007P | FDA UDI | Class II | Active |
| Polypro | 8703P | FDA UDI | Class II | Active |
| Monomid | 919B | FDA UDI | Class II | Active |
| Polybond | CP43A | FDA UDI | Class II | Active |
| Polypro | 8435P | FDA UDI | Class II | Active |
| Polypro | 8840P | FDA UDI | Class II | Active |
| Polypro | 8727P | FDA UDI | Class II | Active |
| Monomid | 944B | FDA UDI | Class II | Active |
| Polypro | 130P | FDA UDI | Class II | Active |
| Polypro | 8843P | FDA UDI | Class II | Active |
| Polypro | 8425P | FDA UDI | Class II | Active |
| Fn Needles | FN17-1T | FDA UDI | Class II | Active |
| Polypro | 8699P | FDA UDI | Class II | Active |
| Polybond | CP869A | FDA UDI | Class II | Active |
| Polypro | 8686P | FDA UDI | Class II | Active |
| Monomid | 668B | FDA UDI | Class II | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (12)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Oct 18, 2019 | Z-0655-2020 | — | open, classified | Failed to meet USP minimum average value for knot pull (tensile) strength. |
| Feb 4, 2019 | Z-1027-2019 | — | open, classified | Potential compromise of product sterility after routine monitoring for Endotoxins showed an out of limit test result. |
| Feb 2, 2017 | Z-1872-2017 | — | open, classified | The tensile strength minimum as directed by USP <881> was not met over the length of the product's shelf life. |
| Sep 22, 2014 | Z-0140-2015 | — | terminated | CP Medical Inc. is recalling five lots of Monoswift PGCL [poly(glycolide-co-caprolactone)] Absorbable Surgical Suture for failing to meet the minimum tensile strength as dictated by USP was not met over the length of the product's shelf life. |
| Apr 23, 2014 | Z-1708-2014 | — | terminated | CP Medical, Inc., is recalling one lot of Monoswift PGCL [poly (glycolide-co-caprolactone)] Absorbable Sutures for failing to meet the USP minimum average value for knot pull (tensile) strength. |
| Jun 29, 2011 | Z-3177-2011 | — | terminated | Unapproved dye was used in manufacturing the non-absorbable blue nylon suture material. |
| Jan 2, 2009 | Z-0260-2012 | — | terminated | The seal integrity of the outer product pouch may be compromised due to partial delamination of the two layers that make up part of the pouch. |
| Jan 2, 2009 | Z-0259-2012 | — | terminated | The seal integrity of the outer product pouch may be compromised due to partial delamination of the two layers that make up part of the pouch. |
| Sep 17, 2008 | Z-2582-2010 | — | terminated | Seal integrity of inner foil pouch of the Mono-Dox Synthetic Absorbable Suture may be compromised. |
| Apr 3, 2007 | Z-0809-2007 | — | terminated | Potential for sterility of product to be compromised. Suture package seals incomplete or missing. |
| Apr 3, 2007 | Z-0808-2007 | — | terminated | Potential for sterility of product to be compromised. Suture package seals incomplete or missing. |
| Apr 3, 2007 | Z-0807-2007 | — | terminated | Potential for sterility of product to be compromised. Suture package seals incomplete or missing. |