VIDENT 90 ALLOY AND VIDENT 95 ALLOY— 510(k) K903008
Substantially EquivalentVident
FDA 510(k) clearance K903008 for VIDENT 90 ALLOY AND VIDENT 95 ALLOY, Substantially Equivalent on 1990-09-06. Applicant: Vident. Device class: 2.
Clearance details
- Applicant
- Vident
- Product code
- Code EJH
- Device class
- Class 2
- Regulation
- 21 CFR 872.3710
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Baldwin Park, CA, US
Recent devices under product code EJH
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- K052710 — VITA VM7, MODEL NX77 XXXX, NX78XXXX, NX79 XXXX; VITA VM 8, MODEL VX60 XXXX, VX61 XXXX, VX62 XXXX; VITA VM 9,
- K052130 — VITA IN-CERAM 2000 AL CUBES FOR INLAB, MODELS AL20/AL40
- K050362 — VITA PM 7 (20 GRAM BOTTLES), VITA PM 7 (50 GRAM BOTTLES)
Data sourced from openFDA. This site is unofficial and independent of the FDA.