# Dinkler Surgical Devices, Inc.

- Location (FDA's records): Dayton, OH
- FDA decisions: 2 (2008–2009): 2 510(k) clearances
- Product codes: HBL (2)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 1 (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
- Ohio Medical Instrument Co., Inc.: 2 (https://510kreport.com/company/ohio-medical-instrument)
- Mizuho America, Inc.: 1 (https://510kreport.com/company/mizuho-america)

## Firms that cite its devices most
- Pro Med Instruments GmbH: 1 (https://510kreport.com/company/pro-med-instruments)

## Its most-cited devices
- K073163: Limited Artifact Skull Pin, Model 0107 (2008), cited by 1

## Recent decisions
- K090695: Dinkler Surgical Skull Clamp, Model 0308 (Apr 23, 2009)
- K073163: Limited Artifact Skull Pin, Model 0107 (Feb 28, 2008)

Source page: https://510kreport.com/company/dinkler-surgical-devices