Sulzer Dental, Inc.
Sulzer Dental, Inc. holds FDA 510(k) medical device clearances, first cleared 2001, most recent 2002.
Top product codes for Sulzer Dental, Inc.
Recent clearances by Sulzer Dental, Inc.
- K014050 — HEX-LOCK TEMPORARY ABUTMENT
- K014175 — SULZER DENTAL CERAMIC SYSTEM-HEXLOCK
- K014214 — SULZER DENTAL CERAMIC SYSTEM-SPLINE
- K013494 — 3.75MM AND 5.0MM SPLINE TWIST IMPLANT
- K013227 — SCREW VENT IMPLANT; TAPERED SCREW VENT IMPLANT
- K012055 — 3.25MM SPLINE TWIST IMPLANT
- K011245 — ADVENT IMPLANT SYSTEM, SWISS PLUS IMPLANT SYSTEM
- K011028 — SCREW-VENT DENTAL IMPLANT SYSTEM
- K011038 — TAPER-LOCK DENTAL IMPLANT SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.