V-Print c&b temp
FDA 510(k) clearance K231591 · decided 2023-07-31
Clearance details
- K-number
- K231591
- Device name
- V-Print c&b temp
- Applicant
- Voco GmbH
- Decision
- Substantially Equivalent
- Date received
- 2023-06-01
- Decision date
- 2023-07-31
- Days to decision
- 60 days
- Clearance type
- Traditional
- Product code
- POW
- Device class
- 2
- Regulation number
- 872.3770
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- Cuxhaven, DE
- 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 |
|---|---|---|
| Ruthinium Disc (K261456) | Dental Manufacturing S.p.A. | 2026-08-05 |
Recalls involving this device
No recalls on record reference this clearance.