# Skanray Technologies Private Limited

- Location (FDA's records): Mysore, IN
- FDA decisions: 4 (2016–2017): 4 510(k) clearances
- Product codes: MWI (1), DXN (1), OXO (1), EHD (1)
- 510(k) review time since 2016: median 193 days, against 101 for FDA's reviews in the same codes and years (0 of 4 faster)
- Predicates its devices cite: 10 (0 its own); citations of its devices by later devices: 1 (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
- Welch Allyn, Inc.: 2 (https://510kreport.com/company/welch-allyn)
- Philips Medical Systems, Inc.: 2 (https://510kreport.com/company/philips-medical-systems)
- Suntech Medical, Inc.: 2 (https://510kreport.com/company/suntech-medical)
- Larsen & Toubro Limited: 2 (https://510kreport.com/company/larsen-toubro)
- Ge Oec Medical Systems, Inc.: 1 (https://510kreport.com/company/ge-oec-medical-systems)
- Skanray Technologies Limited: 1 (https://510kreport.com/company/skanray-technologies)

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

## Its most-cited devices
- K170946: Skan-C Mobile C-Arm X-Ray System - 230V Variant, Skan-C Mobile C-Arm X-Ray System - 110V Variant (2017), cited by 1

## Recent decisions
- K170946: Skan-C Mobile C-Arm X-Ray System - 230V Variant, Skan-C Mobile C-Arm X-Ray System - 110V Variant (Nov 24, 2017)
- K170967: Intraskan DC Plus (Jun 8, 2017)
- K152831: Spot Skan (Feb 23, 2016)
- K151512: Star 60 (Feb 14, 2016)

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