# Powermedic Aps

- Location (FDA's records): Houston, TX
- FDA decisions: 2 (2007–2014): 2 510(k) clearances
- Product codes: ILY (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 5 (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
- Photo Therapeutics Limited: 1 (https://510kreport.com/company/photo-therapeutics)
- Andi Electromedical Aps: 1 (https://510kreport.com/company/andi-electromedical)
- Chattanooga Group, Inc.: 1 (https://510kreport.com/company/chattanooga-group)

## Firms that cite its devices most
- Beijing Huatai Healthcare Technology Co., Ltd.: 1 (https://510kreport.com/company/beijing-huatai-healthcare-technology)
- Biolase Technology, Inc.: 1 (https://510kreport.com/company/biolase-technology)
- Microlight Corporation of America: 1 (https://510kreport.com/company/microlight-of-america)
- Litecure, LLC: 1 (https://510kreport.com/company/litecure)

## Its most-cited devices
- K070516: Powerlaser (2007), cited by 4
- K134017: Gigalaser (2014), cited by 1

## Recent decisions
- K134017: Gigalaser (May 2, 2014)
- K070516: Powerlaser (Jul 2, 2007)

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