# Greiner America, Inc.

- Location (FDA's records): Lake Mary, FL
- FDA decisions: 7 (1996–1997): 7 510(k) clearances
- Product codes: JKA (6), GIM (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (0 its own)
- Recalls linked to its devices: 19 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bd Becton Dickinson Vacutainer Systems Preanalytic: 3 (https://510kreport.com/company/bd-becton-dickinson-vacutainer-systems-preanalytic)

## Firms that cite its devices most
- Greiner Meditech, Inc.: 2 (https://510kreport.com/company/greiner-meditech)
- Greiner Bio-One Vacuette North America: 1 (https://510kreport.com/company/greiner-bio-one-vacuette-north-america)

## Its most-cited devices
- K960858: Greiner Vacutte Blood Collection Tube W/ Clot Activator & Gel Separator (1996), cited by 1
- K971221: Greiner Vacuette Blood Collection Tube (1997), cited by 1
- K960857: Greiner Vacuette Blood Collection Tube W/Lithium Heparin & Gel Separator (1996), cited by 1

## Recent decisions
- K971220: Greiner Vacuette Blood Collection Tube (Jun 4, 1997)
- K971236: Greiner Vacuette Blood Collection Tube (May 12, 1997)
- K971239: Greiner Vacuette Blood Collection Tube (May 12, 1997)
- K971221: Greiner Vacuette Blood Collection Tube (May 2, 1997)
- K960860: Greiner Vacuette Blood Collection Tube E/Edta K3 (Sep 5, 1996)
- K960858: Greiner Vacutte Blood Collection Tube W/ Clot Activator & Gel Separator (Aug 30, 1996)
- K960857: Greiner Vacuette Blood Collection Tube W/Lithium Heparin & Gel Separator (Aug 30, 1996)

Source page: https://510kreport.com/company/greiner-america