# Medi-Tech Intl. Corp.

- Location (FDA's records): Brooklyn, NY
- FDA decisions: 3 (1986–2011): 3 510(k) clearances
- Product codes: FMQ (1), KMF (1), MGQ (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 1 (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
- J. T. Posey Co.: 1 (https://510kreport.com/company/j-t-posey)

## Firms that cite its devices most
- Neutrogena Corp.: 1 (https://510kreport.com/company/neutrogena)

## Its most-cited devices
- K864124: Spand-Gel Granulated Gel (1986), cited by 1

## Recent decisions
- K110377: Protective Restraint (Apr 25, 2011)
- K002666: Diamond Aloe Vera, Sterile (Feb 27, 2001)
- K864124: Spand-Gel Granulated Gel (Nov 26, 1986)

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