510(k) K212254
K212254 is an FDA 510(k) premarket notification submitted by Hdx Will Corp. for the device "DENTRIa series (DENTRIa, DENTRI-Ca, DENTRI-Sa)". The FDA issued a decision of Substantially Equivalent on Oct 19, 2021. The device falls under product code OAS (X-Ray, Tomography, Computed, Dental), a Class II device regulated under 21 CFR 892.1750. Hdx Will Corp. has 8 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 19, 2021
- Date Received
- Jul 19, 2021
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- X-Ray, Tomography, Computed, Dental
- Device Class
- Class II
- Regulation Number
- 892.1750
- Review Panel
- RA
- Submission Type
- 510(k)
Produce cross-sectional diagnostic x-ray images of the intra-oral tissue and teeth.