# Pixxgen Corporation

- Location (FDA's records): Anyang-Si, KR
- FDA decisions: 4 (2018–2021): 4 510(k) clearances
- Product codes: MQB (4)
- 510(k) review time since 2016: median 31 days, against 30 for FDA's reviews in the same codes and years (2 of 4 faster)
- Predicates its devices cite: 3 (2 its own); citations of its devices by later devices: 2 (2 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
- Atlaim Corporation: 1 (https://510kreport.com/company/atlaim)

## Its most-cited devices
- K180976: PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels (2018), cited by 1
- K182533: PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels (2018), cited by 1

## Recent decisions
- K211108: Prudent 1717, Prudent 1417, Prudent 1212 (Jun 4, 2021)
- K190691: Pixx2430 Digital Diagnostic X-Ray Receptor Panel (Apr 4, 2019)
- K182533: PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels (Oct 4, 2018)
- K180976: PIXX 1717; PIXX 1417; PIXX 1212; Digital Diagnostic X-ray Receptor Panels (May 24, 2018)

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