PL Touch PLT
PL Touch PLT is a Class II device made by Erchonia Corporation, cleared under FDA 510(k) K153052 on 4 Jan 2016 and listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00858985006063), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00858985006063 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK153052 | Date4 Jan 2016 | StatusActive |
Official records
- AccessGUDID record 00858985006063
- FDA 510(k) database K153052
Across registries
- FDA 510(k) K153052 decided 4 Jan 2016 Active
- FDA GUDID UDI-DI 00858985006063 listed 24 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K153052
- Listed FDA GUDID 00858985006063
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- PL Touch
- Generic name
- Musculoskeletal/physical therapy laser, professional
- Model / Ref / Catalog
- PLT
- Primary DI / UDI-DI
- 00858985006063
- 510(k) Number
- FDA product code
- NHN
- GMDN term
- Musculoskeletal/physical therapy laser, professional
- Device class
- Class II
- Regulation number
- 890.5500
- GUDID distribution status
- In Commercial Distribution
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