# Faxitron Bioptics, LLC

- Location (FDA's records): Tucson, AZ
- FDA decisions: 5 (2012–2019): 5 510(k) clearances
- Product codes: MWP (5)
- Predicates its devices cite: 11 (5 its own); citations of its devices by later devices: 6 (5 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
- Bioptics, Inc.: 3 (https://510kreport.com/company/bioptics)
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)
- Faxitron X-Ray Corp.: 1 (https://510kreport.com/company/faxitron-x-ray)
- Kub Technologies, Inc.: 1 (https://510kreport.com/company/kub-technologies)

## Firms that cite its devices most
- Clarix Imaging: 1 (https://510kreport.com/company/clarix-imaging)

## Its most-cited devices
- K122428: Faxitron Specien Radiography System (2012), cited by 2
- K153583: BioVision Plus (2016), cited by 2
- K170786: Faxitron Bioptics Speciemen Radiography System (2017), cited by 1
- K173309: Faxitron VisionCT (2018), cited by 1

## Recent decisions
- K183142: PathVisionXL (Mar 14, 2019)
- K173309: Faxitron VisionCT (May 9, 2018)
- K170786: Faxitron Bioptics Speciemen Radiography System (Jul 18, 2017)
- K153583: BioVision Plus (Apr 1, 2016)
- K122428: Faxitron Specien Radiography System (Sep 25, 2012)

Source page: https://510kreport.com/company/faxitron-bioptics