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Sign in to claim this brandCp Medical
US
Last updated May 23, 2026
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Catalogue (435)
Page 5 of 9| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Monoswift | L1093 | FDA UDI | Class II | Active |
| Monoswift | L923 | FDA UDI | Class II | Active |
| Pga | ECN-C120FT | FDA UDI | Class II | Active |
| Cp Fiber | BCPF-20-25 | FDA UDI | Class II | Active |
| Polypro | 8710P | FDA UDI | Class II | Active |
| Visorb | 503A | FDA UDI | Class II | Active |
| Monomid | 795B | FDA UDI | Class II | Active |
| Visorb | 453A | FDA UDI | Class II | Active |
| Polypro | 8685P | FDA UDI | Class II | Active |
| Nylon | MS-60B | FDA UDI | Class II | Active |
| Polypro | 8424P | FDA UDI | Class II | Active |
| Polypro | 8683P | FDA UDI | Class II | Active |
| Visorb Quick | VQ392 | FDA UDI | Class II | Active |
| Mono-Dox | M398 | FDA UDI | Class II | Active |
| Visorb | 345A | FDA UDI | Class II | Active |
| Monomid | 1667B | FDA UDI | Class II | Active |
| Polypro | 8525P | FDA UDI | Class II | Active |
| Polybond | CP52A | FDA UDI | Class II | Active |
| Polypro | 8526P | FDA UDI | Class II | Active |
| Polypro | 8533P | FDA UDI | Class II | Active |
| Visorb | 1092A | FDA UDI | Class II | Active |
| Visorb | 496A | FDA UDI | Class II | Active |
| Polybond | CP581A | FDA UDI | Class II | Active |
| Polypro | 8805P | FDA UDI | Class II | Active |
| Polypro | 8618P | FDA UDI | Class II | Active |
| Power Fiber | CPF-P026 | FDA UDI | Class II | Active |
| Polypro | 8975P | FDA UDI | Class II | Active |
| Poypro | 8521P | FDA UDI | Class II | Active |
| C-Ptfe | 400ERT | FDA UDI | Class II | Active |
| Monomid | 1696B | FDA UDI | Class II | Active |
| Monoswift | L942 | FDA UDI | Class II | Active |
| Cp Fiber | ST657 | FDA UDI | Class II | Active |
| Cp Fiber | ST600 | FDA UDI | Class II | Active |
| Visorb | 466A | FDA UDI | Class II | Active |
| Polypro | 1695P | FDA UDI | Class II | Active |
| Pga | ECN-C130FT | FDA UDI | Class II | Active |
| Polybond | CP77A | FDA UDI | Class II | Active |
| Polybond | CP664A | FDA UDI | Class II | Active |
| Monomid | 1856B | FDA UDI | Class II | Active |
| Poypro | 8680P | FDA UDI | Class II | Active |
| Poypro | 8731P | FDA UDI | Class II | Active |
| Monomid | 1893B | FDA UDI | Class II | Active |
| Silk | 833S-IMC | FDA UDI | Class II | Active |
| Polybond | CP762A | FDA UDI | Class II | Active |
| Visorb | 338A | FDA UDI | Class II | Active |
| Visorb | 391A | FDA UDI | Class II | Active |
| CP Cotton Umbilical Tape | CP12A | FDA UDI | Class I | Active |
| Polybond | CP54A | FDA UDI | Class II | Active |
| Monoswift | L943 | FDA UDI | Class II | Active |
| Monomid | 669B | 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. |