# Agfa-Gevaert, Inc.

- Location (FDA's records): West Germany, DE
- FDA decisions: 4 (1979–2001): 4 510(k) clearances
- Names in FDA's records: Agfa-Gevaert, Inc. (3); Agfa-Gevaert AG (1)
- Product codes: LMC (1), IXW (1), IZH (1), MQB (1)
- Predicates its devices cite: 1 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bayer Corp., Agfa Div.: 1 (https://510kreport.com/company/bayer-agfa-div)

## Firms that cite its devices most
- Agfa Corp.: 3 (https://510kreport.com/company/agfa)
- 3Disc Americas: 1 (https://510kreport.com/company/3disc-americas)
- Cedara Software Corp.: 1 (https://510kreport.com/company/cedara-software)

## Its most-cited devices
- K013138: Adc Compact Plus (2001), cited by 4
- K790273: Mammography System and Cassette (1979), cited by 1

## Recent decisions
- K013138: Adc Compact Plus (Sep 28, 2001)
- K882096: Scopix Video Imager (Aug 9, 1988)
- K832603: Curix Capacity Film Center (Sep 29, 1983)
- K790273: Mammography System and Cassette (Mar 21, 1979)

Source page: https://510kreport.com/company/agfa-gevaert