Laguna Edge (2M) 412005
Laguna Edge (2M) 412005 is a Class I device made by Silhouet-Tone Corporation, listed in FDA GUDID since 12 Nov 2025 (UDI-DI 00667259004007), 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 | Number00667259004007 | Date12 Nov 2025 | StatusListed |
Official records
- AccessGUDID record 00667259004007
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Laguna Edge (2M)
- Generic name
- General examination/treatment chair, electric
- Model / reference
- 412005
- Primary DI / UDI-DI
- 00667259004007
- FDA product code
- LGX
- GMDN term
- General examination/treatment chair, electric
- Device class
- Class I
- Regulation number
- 878.4960
- GUDID distribution status
- In Commercial Distribution
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