# Medi-Flex Hospital Products, Inc.

- Location (FDA's records): Overland Park, KS
- FDA decisions: 13 (1991–1997): 13 510(k) clearances
- Product codes: KMF (3), FMF (2), MCY (1), BTO (1), FRO (1), LRS (1), FOZ (1), KOX (1), LYY (1), FPX (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
- K970441: K-Klosure 2 Inch Length/4 Inch Length/8 Inch Length/12 Inch Length (May 9, 1997)
- K962740: Dermistick Sepp Applicator (200 CT)/(40 CT) 260640/260641 (Sep 6, 1996)
- K952201: Port-a-Cath Access Kit (Oct 4, 1995)
- K952416: Tracheostomy Care Kit (Aug 9, 1995)
- K952256: Picc Line Kit (Jul 31, 1995)
- K952007: Adherol Sepp Applicator (Jun 8, 1995)
- K934790: Sepp Adhesive Remover (Mar 11, 1994)
- K920399: Compound Benzoin Tincture Usp Frepp (Jan 25, 1994)

Source page: https://510kreport.com/company/medi-flex-hospital-products