# Life-Tech Intl., Inc.

- Location (FDA's records): Houston, TX
- FDA decisions: 68 (1982–2000): 68 510(k) clearances
- Product codes: FAP (14), FEN (5), HLX (4), MFD (4), EGJ (4), BXN (3), DXT (3), EXY (3), ETY (2), LIL (2), EAT (2), KOI (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 18 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dynatronics Corp.: 2 (https://510kreport.com/company/dynatronics)
- Mattioli Engineering Corp.: 2 (https://510kreport.com/company/mattioli-engineering)
- Hdc Corp.: 1 (https://510kreport.com/company/hdc)
- Medical Adhesiveonline, LLC: 1 (https://510kreport.com/company/medical-adhesiveonline)
- Rhino Metrics A/S: 1 (https://510kreport.com/company/rhino-metrics-a-s)
- Halyard Health, Inc.: 1 (https://510kreport.com/company/halyard-health)
- Sunmed, Inc.: 1 (https://510kreport.com/company/sunmed)
- Smiths Medical Asd, Inc.: 1 (https://510kreport.com/company/smiths-medical-asd)

## Its most-cited devices
- K882554: Meditrode Kit (1988), cited by 3
- K913184: MS-Iii Ministim (1991), cited by 2
- K913601: Microphor (1994), cited by 2
- K954505: EZ Stim (1996), cited by 2
- K863166: Model 6110 Iontophoretic Applicator (1987), cited by 2
- K823767: Erg-Jet Electrode (1983), cited by 1

## Recent decisions
- K001129: Prolong, Models PL50, PL100, PL150 (Jul 6, 2000)
- K954505: EZ Stim (Dec 10, 1996)
- K955031: Maxistim (Dec 10, 1996)
- K954315: PVC Abdominal/Rectal Pressure Catheter (Nov 30, 1995)
- K954341: Urodynamics Tubing and Infusion Sets (Oct 17, 1995)
- K953451: Uropump Tube & Damping Chamger (Oct 5, 1995)
- K953353: Urovision Janus (Sep 8, 1995)
- K946108: Ear-a-Gator (Jun 13, 1995)

Source page: https://510kreport.com/company/life-tech-intl