Hager& Meisinger GmbH
Hager& Meisinger GmbH holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2025, with 2 FDA device recalls on record.
Top product codes for Hager& Meisinger GmbH
FDA recalls by Hager& Meisinger GmbH
- Z-2937-2020 — SINGLES Carbide US-No. FG556; UDI +E0HM26000313140091; STERILE R; Size 009, Length 3.8; 2025-03-18 - Product Usage: Cutting of hard structures in the mouth, such as teeth or bone, it is also intended to cut hard metals, plastics, porcelains, and similar materials intended for use in the fabrication of dental devices.
- Z-0493-2020 — Singles carbides by Meisinger, US-No: 245, Sterile R, cylinder round end; US-No 245; Reference: HMUN245-009; Shank: FG/314; Head Size 1/10mm: 009,Head Length/mm:
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 Hager& Meisinger GmbH
- K250123 — Master-Pin X (MP Pin with thread) (36BMP000030 / MP30)
- K240321 — MP Pin flat without thread (36BMP000020/MP20)
- K201210 — The Micro Screw System, Micro Screw System Basic
- K173819 — MyPlant II Implant System
- K180360 — OKTAGON Implant System
- K170287 — Dental Implants OKTAGON Bone Level Tapered Design
- K162073 — Dental Implants OKTAGON Tissue Level and Bone Level
- K160132 — Dental Implant Abutment OKTAGON Bone Level RC, Dental Implant Abutment OKTAGON Bone Level NC
- K143539 — Dental Implant OKTAGON Bone Level
- K132214 — ABUTMENT RP, ABUTMENT WP, BURN-OUT COPING, SCREWS, TITANIUM ADHESIVE BASE, ALLIGATOR ABUTMENT, SOLID ABUTMENT, RETENTIVE
- K122807 — DENTAL IMPLANT SYSTEM
- K132212 — DENTAL BONE SCREWS; DENTAL BONE SCREWS, CONTINUING; SCREW SYSTEM TX; SCREW SYSTEM TX PROFESSIONAL
- K130682 — MEISINGER TACS (MEISINGER MEITAC-KIT), MEISINGER PINS (MEISINGER MASTER-PIN-CONTROL-KIT, BASIC-KIT
- K062130 — MEISINGER BENEX, MODEL BE001
Data sourced from openFDA. This site is unofficial and independent of the FDA.