Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in CanadaLabelled 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 14, 2026, FDA's public records list AMD Medicom with 7 device recalls and 2 510(k) clearances. The most recent is a device recall dated May 8, 2026: Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0….
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.
| May 8, 2026 | Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in, Non-Sterile/559Class II · Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to prot | Device recalls |
| May 8, 2026 | Ritmed Neurological Sponges, 0.75x0.75in, Sterile, REF: 85995CClass II · Neurological sponges used to moisten or absorb biological fluid during neurological surgery and may also be used to prot | Device recalls |
| Dec 21, 2023 | PATTERSON¿ PROCEDURE EARLOOP MASKS- ANTI-FOG, ASTM LEVEL 3 (BLUE) (item code 127-7573)Class II · Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initia | Device recalls |
| Dec 21, 2023 | HENRY SCHEIN¿ CRITERION¿ EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-2448)Class II · Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initia | Device recalls |
| Dec 21, 2023 | HENRY SCHEIN¿ CRITERION¿ ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) (item code 570-3281)Class II · Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initia | Device recalls |
| Jan 17, 2020 | AMD Ritmed AssureWear VersaGownK190306 · FYC | 510(k) clearances |
| Oct 11, 2019 | MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 2 MASKS, Item Code 2040Class II · Due to an error on the packaging line, some level 2 masks may have been packed in some level 3 mask boxes. The two masks | Device recalls |
| Oct 11, 2019 | MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 3 MASKS, Item Code 2042Class II · Due to an error on the packaging line, some level 2 masks may have been packed in some level 3 mask boxes. The two masks | Device recalls |
| Sep 17, 2019 | Medicom SafeMask Sofskin Pediatric Procedure Earloop Face Masks (ASTM Level 1), Medicom SafeMask Sofskin Pediatric Procedure Earloop Face Masks, Medicom SafeMask Premier Pediatric Procedure Earloop Face Masks (ASTM Level 1), Medicom SafeMask Premier Pediatric Procedure Earloop Face Masks (ASTM Level 1)K190308 · OXZ | 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
