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Sign in to claim this brandCp Medical
US
Last updated May 23, 2026
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Catalogue (435)
Page 7 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Cp Fiber | CPF-02C | FDA UDI | Class II | Active |
| Polypro | 8976P | FDA UDI | Class II | Active |
| Monoswift | L1015 | FDA UDI | Class II | Active |
| Visorb | 1093A | FDA UDI | Class II | Active |
| Polypro | 8707P | FDA UDI | Class II | Active |
| Pgcl | L347 | FDA UDI | Class II | Active |
| Pga | 302A | FDA UDI | Class II | Active |
| Visorb | 180A | FDA UDI | Class II | Active |
| Fn Needles | FN18-53T | FDA UDI | Class II | Active |
| Polybond | CP25A | FDA UDI | Class II | Active |
| Visorb Quick | VQ494 | FDA UDI | Class II | Active |
| Monoswift | L346 | FDA UDI | Class II | Active |
| Monomid | 1665B | FDA UDI | Class II | Active |
| Polybond | CP977A | FDA UDI | Class II | Active |
| Mono-Dox | M311 | FDA UDI | Class II | Active |
| Monomid | 1674B | FDA UDI | Class II | Active |
| Monomid | 691B | FDA UDI | Class II | Active |
| Monomid | 915B | FDA UDI | Class II | Active |
| Polybond | CP553A | FDA UDI | Class II | Active |
| Visorb | 428A | FDA UDI | Class II | Active |
| Polypro | 8558P | FDA UDI | Class II | Active |
| Visorb | 422A | FDA UDI | Class II | Active |
| Visorb | 269A | FDA UDI | Class II | Active |
| Visorb | 280A | FDA UDI | Class II | Active |
| Monoswift | L922 | FDA UDI | Class II | Active |
| Polypro | 8721P | FDA UDI | Class II | Active |
| Mono-Dox | M467 | FDA UDI | Class II | Active |
| Mono-Dox | M397 | FDA UDI | Class II | Active |
| Visorb | 341A | FDA UDI | Class II | Active |
| Mono-Dox | M334 | FDA UDI | Class II | Active |
| Poypro | 8730P | FDA UDI | Class II | Active |
| Pga | 415A | FDA UDI | Class II | Active |
| Cp Fiber | CPF02 | FDA UDI | Class II | Active |
| Visorb | 452A | FDA UDI | Class II | Active |
| Polypro | 1699P | FDA UDI | Class II | Active |
| Visorb | 464A | FDA UDI | Class II | Active |
| Monoswift | L936 | FDA UDI | Class II | Active |
| Polypro855 | 8556P | FDA UDI | Class II | Active |
| Visorb | 354A | FDA UDI | Class II | Active |
| Visorb | 492A | FDA UDI | Class II | Active |
| Cp Fiber | ST650 | FDA UDI | Class II | Active |
| Polypro | 8926P | FDA UDI | Class II | Active |
| Fn Needles | FN17-3T | FDA UDI | Class II | Active |
| Polypro | 8684P | FDA UDI | Class II | Active |
| Nylon | BDL-50B | FDA UDI | Class II | Active |
| Visorb | 181A | FDA UDI | Class II | Active |
| Polypro | 8977P | FDA UDI | Class II | Active |
| Visorb | 328A | FDA UDI | Class II | Active |
| Polypro | 8687P | FDA UDI | Class II | Active |
| Monomid | 664M | FDA UDI | Class II | Active |
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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. |