Cp Medical, Inc.
Cp Medical, Inc. holds FDA 510(k) medical device clearance, cleared in 2018, with 3 FDA device recalls on record.
Top product codes for Cp Medical, Inc.
FDA recalls by Cp Medical, Inc.
- Z-0655-2020 — Coated PGA Undyed Polyglycolic Acid Braided Absorbable Suture Sterile EO 18" (45cm); UDI: (01)10790986000657 (17)220430 (10)17050970
- Z-1027-2019 — Plain and Chromic Gut Absorbable Surgical Sutures, sterile. 12 sutures per box. Product Usage: Plain Gut Sutures are indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic procedures, but not for use in cardiovascular and neural tissues.
- Z-1872-2017 — PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes L923, L459, L493, L762, L463, L922, L495, L463, L497, L494, L493
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Cp Medical, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.