# Ackermann Instrumente GmbH

- Location (FDA's records): Chesterland, OH
- FDA decisions: 3 (1998–2015): 3 510(k) clearances
- Product codes: FZP (1), ODP (1), GCJ (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 3 (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
- Aesculap Implant Systems, LLC: 2 (https://510kreport.com/company/aesculap-implant-systems)
- Microsurgical Laboratories,Inc.Dba Wexler Surgical: 1 (https://510kreport.com/company/microsurgical-laboratories-dba-wexler-surgical)
- Miltex, Inc.: 1 (https://510kreport.com/company/miltex)
- Genicon, Inc.: 1 (https://510kreport.com/company/genicon)
- Amedica Corp.: 1 (https://510kreport.com/company/amedica)
- Advanced Surgical, Inc.: 1 (https://510kreport.com/company/advanced-surgical)

## Firms that cite its devices most
- Trokamed GmbH: 1 (https://510kreport.com/company/trokamed)
- Flexbar Machine Corp.: 1 (https://510kreport.com/company/flexbar-machine)
- Millennium Devices, Inc.: 1 (https://510kreport.com/company/millennium-devices)

## Its most-cited devices
- K974382: Ackermann Surgical Instruments (1998), cited by 3

## Recent decisions
- K143450: Ackermann Intervertebral Body Fusion Device (Sep 16, 2015)
- K111930: Ackermann Europclip (Nov 8, 2011)
- K974382: Ackermann Surgical Instruments (Apr 21, 1998)

Source page: https://510kreport.com/company/ackermann-instrumente