Core-Vent Corp.
Core-Vent Corp. holds FDA 510(k) medical device clearances, first cleared 1986, most recent 2000.
Top product codes for Core-Vent Corp.
Recent clearances by Core-Vent Corp.
- K002614 — ADVENT IMPLANT SYSTEM
- K002188 — SWISSPLUS IMPLANT SYSTEM, MODEL SPWB 8,10,12,14/OPH20/SMPR, SPB 8,10,12,14/OP3.5D/OPAR,OPB 8,10,12,14/OP2.3D/OP2.8D,
- K950575 — BIO-VENT IMPLANT
- K950576 — BIO-VENT X IMPLANT
- K950577 — SWEDE-VENT IMPLANT
- K950578 — SCREW-VENT IMPLANT
- K950579 — MICRO-VENT IMPLANT
- K912059 — PRE-ANGLED ABUTMENTS
- K913782 — TCAL ABUTMENT
- K910585 — TSIR ANGLED ABUTMENTS
- K902968 — BIO-VENT-X ENDOSSEOUS HA COATED DENTAL IMPLANTS
- K900179 — SCREW-VENT ENDOSSEOUS IMPLANT ABUTMENTS
- K900181 — MICRO-VENT ENDOSSEOUS IMPLANT ABUTMENTS
- K900180 — CORE-VENT ENDOSSEOUS IMPLANT ABUTMENTS
- K902969 — SCREW-VENT ENDOSSEOUS HA COATED DENTAL IMPLANTS
- K900182 — SWEDE-VENT ENDOSSEOUS IMPLANT ABUTMENTS
- K900634 — SWEDE-VENT ENDOSSEOUS HA COATED DENTAL IMPLANTS
- K900177 — CORE-VENT ARMENTARIUM
- K900178 — ELECTRIC MOTOR W/PHYSIO DISPENSER, HANDPIECES
- K883717 — BIO-VENT
- K873255 — THE MICRO-VENT/HA
- K873818 — VENT CORP PIB IMPLANT
- K864321 — MICRO-VENT
- K861425 — SUB-VENT (TM) IMPLANT/ENDOSSEOUS BLADE IMPLANT
- K861426 — SCREW-VENT (TM) IMPLANT/ENDOSSEOUS SCREW IMPLANT
Data sourced from openFDA. This site is unofficial and independent of the FDA.