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Sign in to claim this brandCp Medical
US
Last updated May 23, 2026
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Catalogue (435)
Page 6 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Monomid | 1098B | FDA UDI | Class II | Active |
| Visorb® | 504A | FDA UDI | Class II | Active |
| Fn Needles | FN18-51T | FDA UDI | Class II | Active |
| Pga | 304A | FDA UDI | Class II | Active |
| Visorb | 385A | FDA UDI | Class II | Active |
| Polypro | 8935P | FDA UDI | Class II | Active |
| Monoswift | L345 | FDA UDI | Class II | Active |
| Polypro | 8709P | FDA UDI | Class II | Active |
| Pga | 452A-IMC | FDA UDI | Class II | Active |
| Polypro | 8842P | FDA UDI | Class II | Active |
| Polypro | 8689P | FDA UDI | Class II | Active |
| Monomid | 698B | FDA UDI | Class II | Active |
| Chromic Gut | 122CG-IMC | FDA UDI | Class II | Active |
| Visorb | 392A | FDA UDI | Class II | Active |
| Polybond | CP1080A | FDA UDI | Class II | Active |
| Monomid | 627B | FDA UDI | Class II | Active |
| Monoswift | L762 | FDA UDI | Class II | Active |
| Visorb | 398A | FDA UDI | Class II | Active |
| Polybond | CP938A | FDA UDI | Class II | Active |
| Visorb | 946A | FDA UDI | Class II | Active |
| Visorb | 315A | FDA UDI | Class II | Active |
| Visorb Quick | VQ935 | FDA UDI | Class II | Active |
| Monoswift | L317 | FDA UDI | Class II | Active |
| Monomid | 913B | FDA UDI | Class II | Active |
| Silk | 640SRT | FDA UDI | Class II | Active |
| Visorb | 351A | FDA UDI | Class II | Active |
| Monomid | 1629B | FDA UDI | Class II | Active |
| Visorb Quick | VQ497 | FDA UDI | Class II | Active |
| Monoswift | L316 | FDA UDI | Class II | Active |
| Polypro | 1031P | FDA UDI | Class II | Active |
| Visorb | 310A | FDA UDI | Class II | Active |
| Polypro | 8925P | FDA UDI | Class II | Active |
| Visorb | 282A | FDA UDI | Class II | Active |
| Visorb Quick | VQ391 | FDA UDI | Class II | Active |
| Monomid | 660B | FDA UDI | Class II | Active |
| Visorb | 423A | FDA UDI | Class II | Active |
| Nylon | BDL-60B | FDA UDI | Class II | Active |
| Polypro | 1013P | FDA UDI | Class II | Active |
| Mono-Dox | M341 | FDA UDI | Class II | Active |
| Monoswift | L1016 | FDA UDI | Class II | Active |
| Monomid | 667B | FDA UDI | Class II | Active |
| Visorb | 589A | FDA UDI | Class II | Active |
| Polypro | 8423P | FDA UDI | Class II | Active |
| Visorb | 587A | FDA UDI | Class II | Active |
| Monomid | 1663B | FDA UDI | Class II | Active |
| Polypro | 8720P | FDA UDI | Class II | Active |
| Monomid | 697B | FDA UDI | Class II | Active |
| Visorb | 489A | FDA UDI | Class II | Active |
| Polybond | CP1052A | FDA UDI | Class II | Active |
| Visorb | 495A | 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. |