# Berchtold GmbH & Co. KG

- Location (FDA's records): Charleston, SC
- FDA decisions: 3 (2002–2012): 3 510(k) clearances
- Names in FDA's records: Berchtold GmbH & Co. KG (2); Berchtold Corp. (1)
- Product codes: FSY (2), GEI (1)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 2 (1 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Berchtold Holding GmbH: 1 (https://510kreport.com/company/berchtold-holding)

## Firms that cite its devices most
- Dickson & Dickson Healthcare (Us), Inc.: 1 (https://510kreport.com/company/dickson-dickson-healthcare-us)

## Its most-cited devices
- K090378: Chromophare E 668 (2009), cited by 2

## Recent decisions
- K120392: Chromophare F 628 and F 528 (Feb 16, 2012)
- K090378: Chromophare E 668 (Feb 23, 2009)
- K013668: Berchtold Elektrotom 106 Hitt (Feb 4, 2002)

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