# Skytron, Div. the Kmw Group, Inc.

- Location (FDA's records): Grand Rapids, MI
- FDA decisions: 19 (1981–2007): 19 510(k) clearances
- Product codes: FSY (6), GDC (4), JEA (1), HBN (1), FQO (1), KZF (1), FWY (1), FWW (1), GBC (1), FNM (1), INX (1)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 19 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Medical Illumination International, Inc.: 1 (https://510kreport.com/company/medical-illumination-international)
- Nuvo, Inc.: 1 (https://510kreport.com/company/nuvo)

## Its most-cited devices
- K071698: Aurora Led Series Surgical Lights (2007), cited by 2
- K002463: Stellar (2000), cited by 1

## Recent decisions
- K071698: Aurora Led Series Surgical Lights (Jul 6, 2007)
- K021585: Stellar Series Surgical Lights with Hermes (Nov 13, 2002)
- K002463: Stellar (Nov 8, 2000)
- K992090: Millennium Gold (Sep 8, 1999)
- K950192: Skytron Skyboom Series (Apr 3, 1995)
- K940616: Skytron Elite 3500 Table (Jun 13, 1994)
- K933564: Skytron Exam Light (Feb 10, 1994)
- K926045: Skytron Life Island 21 (Jul 27, 1993)

Source page: https://510kreport.com/company/skytron-div-the-kmw-group