Tekno® 70120-151S
by Tekno Medical Optik-Chirurgie GmbH & Co.
Tekno® 70120-151S is a Class I device made by Tekno Medical Optik-Chirurgie GmbH & Co., listed in FDA GUDID since 19 Oct 2022 (UDI-DI 04044684077817), registry data as of 23 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 | Number04044684077817 | Date19 Oct 2022 | StatusListed |
Official records
- AccessGUDID record 04044684077817
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Tekno®
- Generic name
- Tooth extraction forceps
- Model / Ref / Catalog
- 70120-151S
- Primary DI / UDI-DI
- 04044684077817
- FDA product code
- EMG
- GMDN term
- Tooth extraction forceps
- Device class
- Class I
- Regulation number
- 872.4565
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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