# Burton Medical Products Corp.

- Location (FDA's records): Van Nuys, CA
- FDA decisions: 15 (1985–2010): 15 510(k) clearances
- Product codes: KZF (7), FSY (5), FTD (2), FTA (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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Waldmann Lighting: 1 (https://510kreport.com/company/waldmann-lighting)
- Stryker Communications Corp.: 1 (https://510kreport.com/company/stryker-communications)

## Its most-cited devices
- K042395: Outpatient Iii Minor Surgery Light (2004), cited by 2
- K101537: Aim 200, Major Surgical Light (2010), cited by 1

## Recent decisions
- K101537: Aim 200, Major Surgical Light (Sep 30, 2010)
- K042395: Outpatient Iii Minor Surgery Light (Dec 1, 2004)
- K000639: Visionary 2000 (May 25, 2000)
- K963682: Genie' Single Ceiling and Double Ceiling (Nov 13, 1996)
- K961843: GENIE (Aug 22, 1996)
- K935102: Saturn Light (Jun 27, 1994)
- K942553: Genesis (Jun 23, 1994)
- K936088: Wave Fluorescent Magnifier (Apr 26, 1994)

Source page: https://510kreport.com/company/burton-medical-products