A. Titan Instruments 320.02
A. Titan Instruments 320.02 is a Class I device made by A.Titan Instruments, listed in FDA GUDID since 9 Jan 2023 (UDI-DI 00841685101008), 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 | Number00841685101008 | Date9 Jan 2023 | StatusListed |
Official records
- AccessGUDID record 00841685101008
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- A. Titan Instruments
- Generic name
- Dental osteotome
- Model / reference
- 320.02
- Primary DI / UDI-DI
- 00841685101008
- FDA product code
- DZN
- GMDN term
- Dental osteotome
- Device class
- Class I
- Regulation number
- 872.4565
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Dry Heat Sterilization
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