TruDi Probe TDP0705
TruDi Probe TDP0705 is a multi-purpose stereotactic surgery system (FDA Class II; FDA product code PGW, Ear, Nose, and Throat Stereotaxic Instrument) made by Acclarent, Inc., cleared under FDA 510(k) K193453 on 23 Mar 2020 and listed in FDA GUDID since 31 Jul 2020 (UDI-DI 10705031464209), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10705031464209 | Date31 Jul 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK193453 | Date23 Mar 2020 | StatusActive |
Official records
- AccessGUDID record 10705031464209
- FDA 510(k) database K193453
Across registries
- FDA 510(k) K193453 decided 23 Mar 2020 Active
- FDA GUDID UDI-DI 10705031464209 listed 31 Jul 2020 Listed
Timeline
- Cleared FDA 510(k) K193453
- Listed FDA GUDID 10705031464209
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- TruDi Probe
- Generic name
- Multi-purpose stereotactic surgery system
- Model / Ref / Catalog
- TDP0705
- Primary DI / UDI-DI
- 10705031464209
- 510(k) Number
- FDA product code
- PGW
- GMDN term
- Multi-purpose stereotactic surgery system
- Device class
- Class II
- Regulation number
- 882.4560
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
- Size
- Angle — 70 degree
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