# Emsi

- Location (FDA's records): Alexandria, VA
- FDA decisions: 7 (2008–2022): 7 510(k) clearances
- Names in FDA's records: Emsi (6); Emsi, Inc. (1)
- Product codes: GZJ (3), IPF (3), GXY (1)
- Predicates its devices cite: 7 (1 its own); citations of its devices by later devices: 1 (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
- Johari Digital Healthcare, Ltd.: 1 (https://510kreport.com/company/johari-digital-healthcare)
- Apex Medical Corp.: 1 (https://510kreport.com/company/apex-medical)
- Wholesale Medical Imports, Inc.: 1 (https://510kreport.com/company/wholesale-medical-imports)
- Rs Medical: 1 (https://510kreport.com/company/rs-medical)
- Skylark Device Co., Ltd.: 1 (https://510kreport.com/company/skylark-device)
- Empi: 1 (https://510kreport.com/company/empi)

## Its most-cited devices
- K083030: Tens-Ems-14 (2009), cited by 1

## Recent decisions
- K221958: Flex-MI (Oct 21, 2022)
- K140467: Flex-MT + (Oct 7, 2014)
- K102202: GS 3000 (Nov 23, 2010)
- K090889: Emsi Garment Electrodes (Dec 4, 2009)
- K090717: Flex-Tens (May 8, 2009)
- K083030: Tens-Ems-14 (Feb 5, 2009)
- K071869: Tens/IF 14 (Mar 7, 2008)

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