# Adeor Medical Technologies GmbH

- Location (FDA's records): Pullach, DE
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: HBF (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (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
- Codman & Shurtleff, Inc.: 2 (https://510kreport.com/company/codman-shurtleff)
- Acra Cut, Inc.: 1 (https://510kreport.com/company/acra-cut)

## Recent decisions
- K121253: Meridian Cranial Perforator (Jul 17, 2012)

Source page: https://510kreport.com/company/adeor-medical-technologies