# Medical Action Industries, Inc.

- Location (FDA's records): Arden, NC
- FDA decisions: 8 (1981–2005): 8 510(k) clearances
- Product codes: KKX (1), NAB (1), EFQ (1), HHT (1), GDY (1), HIB (1), FRG (1), GEN (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Itl Corporation Pty, Ltd.: 1 (https://510kreport.com/company/itl)

## Recent decisions
- K042526: Drape, Surgical, X-Ray Element, Models Non Sterile 6120-00, Sterile 704-B, Non Sterile 6124-00X, Sterile 704-BX (Apr 25, 2005)
- K042527: Spatula, Cervical, Cytological, Model 22-9107 (Nov 8, 2004)
- K022948: Vaginal Speculum, Model 5555S, 5555M, or 5555L (Nov 4, 2002)
- K946019: Surgicla Instrument Kit (Mar 20, 1995)
- K923846: Burn Dressing (Sep 11, 1992)
- K884826: Gauze Sponge (Dec 22, 1988)
- K810685: Suture Removal Kit (Mar 26, 1981)
- K810184: Laparotomy Sponge (Feb 4, 1981)

Source page: https://510kreport.com/company/medical-action-industries
