# Biokinemetrics, Inc.

- Location (FDA's records): Carroll, IA
- FDA decisions: 3 (2018–2019): 3 510(k) clearances
- Product codes: MQB (3)
- 510(k) review time since 2016: median 29 days, against 30 for FDA's reviews in the same codes and years (3 of 3 faster)
- Predicates its devices cite: 4 (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
- Iray Technology Taicang, Ltd.: 2 (https://510kreport.com/company/iray-technology-taicang)
- Imaging Dynamics Company, Ltd.: 1 (https://510kreport.com/company/imaging-dynamics)
- Imasight, Inc.: 1 (https://510kreport.com/company/imasight)

## Recent decisions
- K190300: BIOK7600W Wireless Flat Panel Detector (Mar 13, 2019)
- K190311: BIOK7600 Flat Panel Detector (Mar 13, 2019)
- K181565: Aquarius 8600 Digital Radiography Sensor (Jul 13, 2018)

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