Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 3 spellings of its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Avid Medical, Inc. with 209 device recalls and 2 510(k) clearances. The most recent is a device recall dated Apr 9, 2021: FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020..
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.
| Apr 9, 2021 | FISTULA ON-OFF KIT. Medical convenience kit, Avid Medical Part Number: MMTN020.Class I · Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD Ch | Device recalls |
| Apr 9, 2021 | DIALYSIS ACCESS Medical convenience kit, Avid Medical Part Number: VMED004-03.Class I · Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD Ch | Device recalls |
| Apr 9, 2021 | ADULT CHEST TUBE TRAY. Medical convenience kit, Avid Medical Part Number: LAKC001-04Class I · Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD Ch | Device recalls |
| Apr 9, 2021 | FISTULA (ON/OFF) ALL IN ONE BAG. Medical convenience kit, Avid Medical Part Number: VAMK024-03Class I · Medical convenience kits are being recalled due to a potential breach in the package integrity of a component, the BD Ch | Device recalls |
| Feb 18, 2020 | Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgerieClass II · The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that | Device recalls |
| Feb 18, 2020 | Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgerieClass II · The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that | Device recalls |
| Feb 18, 2020 | Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgerieClass II · The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that | Device recalls |
| Feb 18, 2020 | Custom procedure trays containing medical components needed to facilitate patient procedures and to perform minor and major patient surgerieClass II · The medical procedure trays contain one or more recalled surgical gowns. The gowns were manufactured at locations that | Device recalls |
| Aug 29, 2000 | AVID-NIT LOSS OF RESISTANCE SYRINGEK001731 · FMF | 510(k) clearances |
| Apr 13, 2000 | AVID-NIT CERVICAL REGIONAL ANESTHESIA NEEDLEK000117 · HEE | 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
