Flat Window PRD-000233-000-L
by Litecure LLC
Flat Window PRD-000233-000-L is a Class II device made by Litecure LLC, listed in FDA GUDID since 30 Jun 2022 (UDI-DI 00854103007233), 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 | Number00854103007233 | Date30 Jun 2022 | StatusListed |
Official records
- AccessGUDID record 00854103007233
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Flat Window
- Generic name
- Musculoskeletal/physical therapy laser beam guide tip, transcutaneous
- Model / reference
- PRD-000233-000-L
- Primary DI / UDI-DI
- 00854103007233
- FDA product code
- ILY
- GMDN term
- Musculoskeletal/physical therapy laser beam guide tip, transcutaneous
- Device class
- Class II
- Regulation number
- 890.5500
- GUDID distribution status
- In Commercial Distribution
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