Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 5 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list CP Medical with 32 510(k) clearances and 5 device recalls. The most recent is a 510(k) clearance dated Mar 26, 2018: C-PTFETM Surgical Suture.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 26, 2018 | C-PTFETM Surgical SutureK173922 · NBY | 510(k) clearances |
| Sep 22, 2014 | Monoswift PGCL [poly(glycolide-co-caprolactone)] Absorbable Surgical Suture; USP size 3/0. Product is labeled sterile. The product is sealClass II · CP Medical Inc. is recalling five lots of Monoswift PGCL [poly(glycolide-co-caprolactone)] Absorbable Surgical Suture fo | Device recalls |
| Mar 18, 2010 | CP-FIBER (ORTHOFIBER)K094028 · GAT | 510(k) clearances |
| Oct 5, 2007 | MONOSWIFTK072229 · GAM | 510(k) clearances |
| Jul 18, 2007 | PRE-WAXED NEEDLES WITH GOLD FIDUCIARY MARKERSK071550 · KXK | 510(k) clearances |
| Nov 2, 2006 | OSCERA7 SYNTHETIC ABSORBABLE BONE WAX, MODEL OS31K060987 · MTJ | 510(k) clearances |
| Sep 17, 2004 | ORTHOFIBERK041894 · GAT | 510(k) clearances |
| Jan 30, 2004 | CP SLEEVE AND RIVER SLEEVEK034062 · KXK | 510(k) clearances |
| Jun 19, 2003 | CP MEDICAL BONE WAXK024372 · MTJ | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
