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 its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Meadox Surgimed, Inc. with 24 510(k) clearances. The most recent is a 510(k) clearance dated Mar 13, 1995: MS CLASSIQUE BALLOON CATHETER.
| Mar 13, 1995 | MS CLASSIQUE BALLOON CATHETERK944143 · FGE | 510(k) clearances |
| Mar 9, 1995 | NOPROFILE OLBERT CATHETER SYSTEMK945061 · KOD | 510(k) clearances |
| Aug 22, 1994 | MS AMPLATZ EXTRA STIFF GUIDE WIREK942382 · DQX | 510(k) clearances |
| Jun 9, 1993 | ACECUT SUTOMATIC BIOPSY SYSTEMK930201 · KNW | 510(k) clearances |
| Jun 20, 1991 | MEADOX(R) SURGIMED(R) BIOPSY GUN IIK911635 · KNW | 510(k) clearances |
| Mar 6, 1991 | NO PROFILE OLBERT CATHETER SYSTEM FOR UROLOGYK905181 · EZN | 510(k) clearances |
| Feb 25, 1991 | QUICKWIRE - HYDROPHILIC COATED GUIDEWIREK904582 · DQX | 510(k) clearances |
| Jan 30, 1991 | MEADOX(R) SURGIMED OLBERT CATH SYST FOR UROLOGYK904983 · EZN | 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
