# Alphamed, Inc.

- Location (FDA's records): El Paso, TX
- FDA decisions: 4 (1993–2019): 4 510(k) clearances
- Product codes: FRW (1), MNR (1), HOZ (1), LZU (1)
- Predicates its devices cite: 3 (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
- Edentec Corp.: 1 (https://510kreport.com/company/edentec)
- Pro-Tech, Inc.: 1 (https://510kreport.com/company/pro-tech)
- Lacrimedics, Inc.: 1 (https://510kreport.com/company/lacrimedics)

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

## Its most-cited devices
- K990321: Alphamed Gemini Sensor, Snoring Sensor (1999), cited by 1

## Recent decisions
- K190210: Tear Pool Dissolvable Punctum Plugs (Oct 24, 2019)
- K091240: Alphamed Surgical Spear, Model 70-5000 (Oct 23, 2009)
- K990321: Alphamed Gemini Sensor, Snoring Sensor (Jun 1, 1999)
- K926446: EZ Pump (Sep 27, 1993)

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