Calcitek, Inc.
Calcitek, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 1997.
Top product codes for Calcitek, Inc.
Recent clearances by Calcitek, Inc.
- K962576 — SPLINE X ENDOSSEOUS DENTAL IMPLANT SYSTEM
- K962106 — SPLINE DENTAL IMPLANT SYSTEMS
- K955619 — 5.0MM SPLINE ENDOSSEOUS DENTAL IMPLANT SYSTEMS
- K943604 — INTEGRAL V BIOINTEGRATED DENTAL IMPLANT SYSTEM
- K960021 — CALCITEK HA-COATED ENDOSSEOUS DENTAL IMPLANT SYSTEMS
- K946319 — INTEGRAL VII 4.9MM BIOINTEGRATED DENTAL IMPLANT SYSTEM
- K946345 — INTEGRAL VIII BIOINTEGRATED DENTAL IMPLANT SYSTEM
- K946311 — INTEGRAL VII 3.25MM BIOINTEGRATED DENTAL IMPLANT SYSTEM
- K943180 — INTEGRAL IV BIOINTEGRATED DENTAL IMPLANT SYSTEM
- K944327 — INTEGRAL VI BIOINTEGRATED DENTAL IMPLANT SYSTEM
- K941608 — INTEGRAL OMNILOC DENTAL IMPLANT WITH INTERFACE RING
- K925490 — INTEGRAL III BIOINTEGRATED DENTAL IMPLANT SYSTEM
- K931440 — CALCITEK TORQUE WRENCH SYSTEM
- K923562 — INTERGRAL III DENTAL IMPLANT SYSTEM
- K932274 — INTEGRAL III DENTAL IMPLANT ABUTMENT
- K915597 — BUR,DENTAL (76EJL)
- K900694 — CASTABLE ABUTMENTS
- K900549 — INTEGRAL PLUS BIOINTEGRATED DENTAL IMPLANT SYSTEM
- K900545 — O-RING PROSTHETIC ATTACHMENT DEVICE
- K852682 — CALCITITE BONE GRAFT MAT/ORAL & MAXILLOFACIAL SURG
- K840750 — HYDROXYLAPATITE COATED ENDOSSEOUS DENT
Data sourced from openFDA. This site is unofficial and independent of the FDA.