# Skanray Technologies Limited

- Location (FDA's records): Mysore, IN
- FDA decisions: 6 (2011–2025): 6 510(k) clearances
- Names in FDA's records: Skanray Technologies Limited (4); Skanray Technologies (2)
- Product codes: EHD (2), KPR (2), IZL (1), OWB (1)
- 510(k) review time since 2016: median 152 days, against 83 for FDA's reviews in the same codes and years (1 of 4 faster)
- Predicates its devices cite: 13 (1 its own); citations of its devices by later devices: 2 (1 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
- Progeny, Inc.: 2 (https://510kreport.com/company/progeny)
- Gendex Corp.: 2 (https://510kreport.com/company/gendex)
- Dentsply Intl.: 2 (https://510kreport.com/company/dentsply-intl)
- Shimadzu Corp.: 1 (https://510kreport.com/company/shimadzu)
- Arquilla, Inc. Dba X-Cel X-Ray Corporation: 1 (https://510kreport.com/company/arquilla-dba-x-cel-x-ray)
- Oehm Und Rehbein GmbH: 1 (https://510kreport.com/company/oehm-und-rehbein)
- Sedecal., Sa.: 1 (https://510kreport.com/company/sedecal)
- DRTECH Corporation: 1 (https://510kreport.com/company/drtech)

## Firms that cite its devices most
- Skanray Technologies Private Limited: 1 (https://510kreport.com/company/skanray-technologies-private)

## Its most-cited devices
- K111330: Air Techniques High Frequency Intra-Oral X-Ray (2011), cited by 1
- K103579: Intra Skan DC (2011), cited by 1

## Recent decisions
- K251893: Skan C Pulsar (Dec 16, 2025)
- K231761: PodSKAN HF Diagnostic X-ray System (Oct 27, 2023)
- K220518: Skanrad 400 (Apr 1, 2022)
- K212940: Skanmobile, Skanmobile-Dr (Mar 4, 2022)
- K111330: Air Techniques High Frequency Intra-Oral X-Ray (May 27, 2011)
- K103579: Intra Skan DC (Mar 18, 2011)

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