Midmark Dental Delivery System— 510(k) K251626
Substantially EquivalentMidmark Corporation
FDA 510(k) clearance K251626 for Midmark Dental Delivery System, Substantially Equivalent on 2025-11-03. Applicant: Midmark Corporation. Device class: 1.
Clearance details
- Applicant
- Midmark Corporation
- Product code
- Code EIA
- Device class
- Class 1
- Regulation
- 21 CFR 872.6640
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Versailles, OH, US
Recent devices under product code EIA
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- K163337 — Midmark and Ritter M9 and M11 UltraClave® Automatic Sterilizers and Ritter M9D AutoClave® Automatic Sterilizer
- K161909 — IQvitals Zone
Data sourced from openFDA. This site is unofficial and independent of the FDA.