# Berchtold Holding GmbH

- Location (FDA's records): Tuttlingen, DE
- FDA decisions: 16 (1992–2008): 16 510(k) clearances
- Product codes: FSY (9), GEI (3), FQO (2), KZF (1), KMI (1)
- Predicates its devices cite: 7 (7 its own); citations of its devices by later devices: 15 (7 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
- Medical Illumination International, Inc.: 2 (https://510kreport.com/company/medical-illumination-international)
- Alm Surgical Equipment, Inc.: 1 (https://510kreport.com/company/alm-surgical-equipment)
- Stryker Endoscopy: 1 (https://510kreport.com/company/stryker-endoscopy)
- Conmed Integrated Systems, Canada, Ulc: 1 (https://510kreport.com/company/conmed-integrated-systems-canada-ulc)
- Berchtold GmbH & Co. KG: 1 (https://510kreport.com/company/berchtold)
- Trumpf Kreuzer Medizin Systeme GmbH + Co.Kg: 1 (https://510kreport.com/company/trumpf-kreuzer-medizin-systeme)
- Mavig GmbH: 1 (https://510kreport.com/company/mavig)

## Its most-cited devices
- K965130: Chromophare (1997), cited by 4
- K024132: Chromophare X 65 (2003), cited by 3
- K083066: Chromophare E 778 and E 558 (2008), cited by 3
- K922836: Chromophare (1992), cited by 2
- K080857: Chromophare E-Series (2008), cited by 1
- K974433: Chromophare D 500, Chromophare D 530 (1998), cited by 1

## Recent decisions
- K083066: Chromophare E 778 and E 558 (Oct 30, 2008)
- K080857: Chromophare E-Series (Apr 10, 2008)
- K024132: Chromophare X 65 (Mar 21, 2003)
- K990656: Chromophare D 530 LDR Surgical Light (Jul 20, 1999)
- K991527: Chromophare D500, D530, D650 (May 27, 1999)
- K974433: Chromophare D 500, Chromophare D 530 (Feb 20, 1998)
- K965130: Chromophare (Jul 14, 1997)
- K955750: Teletom (Feb 8, 1996)

Source page: https://510kreport.com/company/berchtold-holding