# Medi Tex, Inc.

- Location (FDA's records): New York, NY
- FDA decisions: 4 (1984–1992): 4 510(k) clearances
- Product codes: LYY (3), FMI (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
- K923901: Latex Examination Gloves (Dec 4, 1992)
- K901116: Sterile Latex Patient Examination Gloves (Apr 25, 1990)
- K891298: Ambiderm (TM) Patient Examination Glove (Latex) (Mar 29, 1989)
- K840944: Infusion Needle Iipn (Apr 13, 1984)

Source page: https://510kreport.com/company/medi-tex