PowerLaser Pro500 probe 2120
PowerLaser Pro500 probe 2120 is a musculoskeletal/physical therapy laser (FDA Class II; FDA product code ILY, Lamp, Infrared, Therapeutic Heating) made by Powermedic ApS, listed in FDA GUDID since 22 Nov 2016 (UDI-DI 05713592021203), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05713592021203 | Date22 Nov 2016 | StatusListed |
Official records
- AccessGUDID record 05713592021203
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PowerLaser Pro500 probe
- Generic name
- Musculoskeletal/physical therapy laser, home-use
- Model / reference
- 2120
- Primary DI / UDI-DI
- 05713592021203
- FDA product code
- ILY
- GMDN term
- Musculoskeletal/physical therapy laser, home-use
- Device class
- Class II
- Regulation number
- 890.5500
- GUDID distribution status
- In Commercial Distribution
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