# Kentron Health Care, Inc.

- Location (FDA's records): Hollywood, FL
- FDA decisions: 6 (1995–2003): 6 510(k) clearances
- Product codes: FYC (2), GDY (1), HIB (1), FLK (1), EFQ (1)
- Predicates its devices cite: 0 (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 that cite its devices most
- Gynova, LLC: 1 (https://510kreport.com/company/gynova)

## Its most-cited devices
- K030693: Kentex Disposable Vaginal Speculum (2003), cited by 1

## Recent decisions
- K030693: Kentex Disposable Vaginal Speculum (Aug 27, 2003)
- K971917: Kentron's Isolation Gown (Sep 19, 1997)
- K972410: Impervious Isolation Gown (Sep 19, 1997)
- K953465: Kentemp (Dec 15, 1995)
- K953914: Kentex (Nov 6, 1995)
- K953830: Kensorb (Oct 3, 1995)

Source page: https://510kreport.com/company/kentron-health-care