DistributorLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list MPM Medical LLC with 9 510(k) clearances and 1 drug recall. The most recent is a drug recall dated Nov 17, 2020: REGENECARE HA (Lidocaine HCL 2%) Topical Anesthetic Hydrogel, Net Wt. 3 oz. (85 g), Man….
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.
| Nov 17, 2020 | REGENECARE HA (Lidocaine HCL 2%) Topical Anesthetic Hydrogel, Net Wt. 3 oz. (85 g), Manufactured For: MPM Medical Mesquite, TX 75149. NDC 6Class I · Microbial Contamination of Non-Sterile Drug Product. The product was found to be contaminated with the bacteria Burkhold | Drug recalls |
| May 10, 2006 | ORAMAGIC PLUS ORAL WOUND RINSEK060340 · OLR | 510(k) clearances |
| Mar 14, 2003 | ORAMAGICRX ORAL WOUND RINSEK024180 · OLR | 510(k) clearances |
| Nov 1, 2002 | REGENECARE WOUND GELK020540 · SEJ | 510(k) clearances |
| Dec 23, 1999 | MPM REGENECARE WOUND GELK992074 · MGQ | 510(k) clearances |
| Jun 26, 1996 | MPM HYDROGEL DRESSING (NON-STERILE)K962160 · MGQ | 510(k) clearances |
| Jun 30, 1995 | MPM HYDROGEL DRESSINGK952276 · MGQ | 510(k) clearances |
| Jul 11, 1994 | MPM HYDROGELK942798 · MGQ | 510(k) clearances |
| Jul 8, 1993 | MPM HYDROGEL SATURATED DRESSINGK930560 · MGQ | 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
