Midmark Corporation
Midmark Corporation holds FDA 510(k) medical device clearances, first cleared 2016, most recent 2026, with 2 FDA device recalls on record.
Top product codes for Midmark Corporation
FDA recalls by Midmark Corporation
- Z-3013-2026 — Midmark Digital ECG HD+12, HD+15, Model/Catalog Number: 4-000-0080 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.
- Z-3012-2026 — Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Midmark Corporation
- K253196 — Midmark 800 Digital Vital Signs Device (1-300-0100, 1-300-0200, 1-300-0300, 1-300-0400)
- K251626 — Midmark Dental Delivery System
- K233026 — Midmark Smart M9® Sterilizer, Midmark Smart M11® Sterilizer
- K201667 — Midmark Extraoral Imaging System (EOIS)
- 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.