# Oriental Inspiration Limited

- Location (FDA's records): Hong Kong, CN
- FDA decisions: 6 (2004–2024): 6 510(k) clearances
- Names in FDA's records: Oriental Inspiration Limited (5); Oriental Inspiration, Ltd. (1)
- Product codes: KPI (1), OHT (1), GZJ (1), FLL (1), OLP (1), NUH (1)
- 510(k) review time since 2016: median 154 days, against 181 for FDA's reviews in the same codes and years (2 of 5 faster)
- Predicates its devices cite: 6 (0 its own); citations of its devices by later devices: 2 (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
- El Global Trade, Ltd.: 1 (https://510kreport.com/company/el-global-trade)
- Home Skinovations, Ltd.: 1 (https://510kreport.com/company/home-skinovations)
- Idt Technology Limited: 1 (https://510kreport.com/company/idt-technology)
- Led Intellectual Properties, LLC: 1 (https://510kreport.com/company/led-intellectual-properties)
- Michael Todd, LP: 1 (https://510kreport.com/company/michael-todd)
- Biorenew Labs, LLC: 1 (https://510kreport.com/company/biorenew-labs)

## Firms that cite its devices most
- Luminance Medical Ventures, Inc.: 1 (https://510kreport.com/company/luminance-medical-ventures)
- Shenzhen Ionka Medical Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-ionka-medical-technology)

## Its most-cited devices
- K170269: Hee HR Mini (2017), cited by 1
- K170260: BC-001+ Acne Purifier (2017), cited by 1

## Recent decisions
- K233046: Electrical Neuromuscular Stimulator, Cure Trio (Apr 19, 2024)
- K213133: Keffort (MC-100, MC-100A) (Apr 13, 2022)
- K212285: Electrical Neuromuscular Stimulator (Cure Trio MC-310 iOS, Cure Trio MC-310 Android) (Dec 22, 2021)
- K170269: Hee HR Mini (May 3, 2017)
- K170260: BC-001+ Acne Purifier (Apr 25, 2017)
- K032612: IR Forehead Thermometer, Model HV-T36 (Feb 19, 2004)

Source page: https://510kreport.com/company/oriental-inspiration