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Sign in to claim this brandCp Medical
US
Last updated May 23, 2026
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Catalogue (435)
Page 2 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mono-Dox | M333 | FDA UDI | Class II | Active |
| Visorb | U386A | FDA UDI | Class II | Active |
| Visorb | 311A | FDA UDI | Class II | Active |
| Polypro | 8635P | FDA UDI | Class II | Active |
| Nylon | 1667B | FDA UDI | Class II | Active |
| Monomid | 663B | FDA UDI | Class II | Active |
| Monomid | 662B | FDA UDI | Class II | Active |
| Mono-Dox | M315 | FDA UDI | Class II | Active |
| Monoswift | L494 | FDA UDI | Class II | Active |
| Visorb | 316A | FDA UDI | Class II | Active |
| Polypropylene | 8384P | FDA UDI | Class II | Active |
| Visorb Quick | VQ936 | FDA UDI | Class II | Active |
| Visorb | 427A | FDA UDI | Class II | Active |
| Mono-Dox | M338 | FDA UDI | Class II | Active |
| Polypro | 8523P | FDA UDI | Class II | Active |
| Visorb | 426A | FDA UDI | Class II | Active |
| Fn Needles | FN18-1T | FDA UDI | Class II | Active |
| Polypro | 8735P | FDA UDI | Class II | Active |
| Visorb | 602A | FDA UDI | Class II | Active |
| Polybond | CP976A | FDA UDI | Class II | Active |
| Polypro | 8422P | FDA UDI | Class II | Active |
| Visorb | 467A | FDA UDI | Class II | Active |
| Visorb | 683A | FDA UDI | Class II | Active |
| Monoswift | L493 | FDA UDI | Class II | Active |
| Polypro | 8557P | FDA UDI | Class II | Active |
| Polybond | CP23A | FDA UDI | Class II | Active |
| Silk | 1862S | FDA UDI | Class II | Active |
| Visorb | 463A | FDA UDI | Class II | Active |
| Polypro | 8807P | FDA UDI | Class II | Active |
| Polybond | CP35A | FDA UDI | Class II | Active |
| Visorb | 417A | FDA UDI | Class II | Active |
| Nylon | 663B | FDA UDI | Class II | Active |
| Visorb | 281A | FDA UDI | Class II | Active |
| Monomid | 662M | FDA UDI | Class II | Active |
| Mono-Dox | M466 | FDA UDI | Class II | Active |
| Polypro | 1698P | FDA UDI | Class II | Active |
| Nylon | MS-50B | FDA UDI | Class II | Active |
| Visorb | 845A | FDA UDI | Class II | Active |
| Monoswift | L427 | FDA UDI | Class II | Active |
| Polypro | 8831P | FDA UDI | Class II | Active |
| Monoswift | L987 | FDA UDI | Class II | Active |
| Monoswift | L1026 | FDA UDI | Class II | Active |
| Visorb Quick | VQ496 | FDA UDI | Class II | Active |
| Monoswift | L426 | FDA UDI | Class II | Active |
| Visorb | 493A | FDA UDI | Class II | Active |
| Monoswift | L845 | FDA UDI | Class II | Active |
| Monomid | 738B | FDA UDI | Class II | Active |
| Mono-Dox | M0112 | FDA UDI | Class II | Active |
| Visorb | 352A | FDA UDI | Class II | Active |
| Visorb | 936A | 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. |