# Aemed, Inc.

- Location (FDA's records): South Miami, FL
- FDA decisions: 2 (2008–2014): 2 510(k) clearances
- Product codes: GZJ (1), NUH (1)
- Predicates its devices cite: 5 (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
- Gemore Technology Co, Ltd.: 1 (https://510kreport.com/company/gemore-technology)
- Innovative Designer Products, Inc.: 1 (https://510kreport.com/company/innovative-designer-products)
- Medipoint, Ltd.: 1 (https://510kreport.com/company/medipoint)
- Hi-Dow International, Inc.: 1 (https://510kreport.com/company/hi-dow-international)

## Firms that cite its devices most
- Neuromed Devices, Inc.: 1 (https://510kreport.com/company/neuromed-devices)

## Its most-cited devices
- K071120: Aemed Stimpad Acu-Tens Transcutaneous Electrical Nerve Stimulator, Model 021999 (2008), cited by 2

## Recent decisions
- K142686: StimPad OTC (Dec 18, 2014)
- K071120: Aemed Stimpad Acu-Tens Transcutaneous Electrical Nerve Stimulator, Model 021999 (Mar 13, 2008)

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