Vita Zahnfabrik H.Rauter GmbH & Co.
Brea, CA, US
Vita Zahnfabrik H.Rauter GmbH & Co. appears in FDA device records in Brea, CA. FDA records list 8 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 8
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 8 510(k) clearances for Vita Zahnfabrik H.Rauter GmbH & Co. between 2009 and 2025. The busiest year on record is 2009, with 1. The most recent is 2025, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2009 | 1 |
| 2010 | 1 |
| 2012 | 1 |
| 2014 | 1 |
| 2015 | 1 |
| 2016 | 1 |
| 2018 | 1 |
| 2025 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K243940 | VITA YZ Multi Translucent | EIH | Substantially Equivalent | |
| K180703 | VITA YZ ST and VITA YZ XT | EIH | Substantially Equivalent | |
| K153645 | VITA ENAMIC Implant Solutions (IS) | NHA | Substantially Equivalent | |
| K152373 | VITA VM LC Flow | EBF | Substantially Equivalent | |
| K132070 | VITA SUPRINITY(R) | EIH | Substantially Equivalent | |
| K122269 | ENAMIC | EIH | Substantially Equivalent | |
| K102128 | VITABLOCS | EIH | Substantially Equivalent | |
| K090644 | VITABLOCS, MODEL VX55-**** | EIH | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain