Guided Surgery 260-101-835
by Bicon, LLC
Guided Surgery 260-101-835 is a Class I device made by Bicon, LLC, listed in FDA GUDID since 10 Jun 2016 (UDI-DI 00813110024541), 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 | Number00813110024541 | Date10 Jun 2016 | StatusListed |
Official records
- AccessGUDID record 00813110024541
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Guided Surgery
- Generic name
- Dental implant/prosthesis surgical procedure kit
- Model / Ref / Catalog
- 260-101-835
- Primary DI / UDI-DI
- 00813110024541
- FDA product code
- NDP
- GMDN term
- Dental implant/prosthesis surgical procedure kit
- Device class
- Class I
- Regulation number
- 872.3980
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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