ToothWave™
FDA 510(k) clearance DEN190039 · decided 2020-09-17
Clearance details
- K-number
- DEN190039
- Device name
- ToothWave™
- Applicant
- Home Skinovations , Ltd.
- Decision
- Unknown
- Date received
- 2019-08-22
- Decision date
- 2020-09-17
- Days to decision
- 392 days
- Clearance type
- Direct
- Product code
- QMJ
- Device class
- 2
- Regulation number
- 872.6866
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Yokneam, IL
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Silk’n Toothwave (K214078) | Home Skinovations , Ltd. | 2023-01-13 |
Recalls involving this device
No recalls on record reference this clearance.