# Kub Technologies, Inc.

- Location (FDA's records): Stratford, CT
- FDA decisions: 10 (2007–2021): 10 510(k) clearances
- Product codes: MWP (6), MQB (2), IZL (1), KPR (1)
- 510(k) review time since 2016: median 164 days, against 154 for FDA's reviews in the same codes and years (0 of 4 faster)
- Predicates its devices cite: 17 (7 its own); citations of its devices by later devices: 9 (7 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
- Hologic, Inc.: 3 (https://510kreport.com/company/hologic)
- Siemens Medical Solutions USA, Inc.: 2 (https://510kreport.com/company/siemens-medical-solutions-usa)
- Canon, Inc.: 1 (https://510kreport.com/company/canon)
- Perkinelmer, Inc.: 1 (https://510kreport.com/company/perkinelmer)
- Bioptics, Inc.: 1 (https://510kreport.com/company/bioptics)
- Faxitron X-Ray Corp.: 1 (https://510kreport.com/company/faxitron-x-ray)
- Micro-Focus Imaging., Inc.: 1 (https://510kreport.com/company/micro-focus-imaging)

## Firms that cite its devices most
- Hologic, Inc.: 1 (https://510kreport.com/company/hologic)
- Faxitron Bioptics, LLC: 1 (https://510kreport.com/company/faxitron-bioptics)

## Its most-cited devices
- K071233: Xpert 40 Specimen Radiography System (2007), cited by 5
- K183624: Kubtec Mozart (Xpert42) (2019), cited by 2
- K083510: Kubtec Xpert 20 (2009), cited by 1
- K200756: Kubtec Mozart Supra (2020), cited by 1

## Recent decisions
- K210955: Kubtec Mozart Supra (XPERT 84) Radiography System (Sep 20, 2021)
- K210957: Kubec Xpert 80 Radiography System (Aug 31, 2021)
- K210956: Kubtec Mozart (XPERT42) (Aug 31, 2021)
- K200756: Kubtec Mozart Supra (Jun 12, 2020)
- K183624: Kubtec Mozart (Xpert42) (Jun 20, 2019)
- K151221: Kubtec DIGIVIEW 395 (Jun 23, 2015)
- K141539: Kubtec X250 (Oct 29, 2014)
- K103348: Digiview 250 (Oct 20, 2011)

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