# Medspec Corp.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 15 (1980–1981): 15 510(k) clearances
- Product codes: GDY (4), KKX (2), FQM (1), LDQ (1), EFN (1), NAB (1), FRL (1), GBS (1), CAE (1), FYC (1)
- Predicates its devices cite: 0 (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

## Recent decisions
- K813012: Sterile Basin Sets (Nov 6, 1981)
- K812711: Sterile Gauze Pads 12PLY (Nov 2, 1981)
- K812710: Sterile Laparotomy Sponges-X-Ray Detect (Nov 2, 1981)
- K812707: Sterile Dissector Sponges-X-Ray Detect (Nov 2, 1981)
- K812709: Sterile Dental Roll (Oct 23, 1981)
- K810071: Sterile Silicone Tubing (Feb 12, 1981)
- K810069: Sterile Airway (Feb 2, 1981)
- K802060: Sterile Tonsil Sponges (Oct 10, 1980)

Source page: https://510kreport.com/company/medspec