Carbomedics, Inc.
Carbomedics, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 1997.
Top product codes for Carbomedics, Inc.
Recent clearances by Carbomedics, Inc.
- K970375 — ANNULOFLO SYSTEM
- K964665 — VASCUTEK GELWEAVE VASCULAR GRAFT (BIFURCATED CONFIGURATION)
- K962154 — CARBOMEDICS HANDLE
- K960923 — CARBOMEDICS MITRAL ROTATOR
- K960706 — VASCUTEK VASCUSOFT PLUS VASCULAR GRAFT
- K960169 — CARBOMEDICS VALVE TESTER
- K955588 — VASCUTEK GRAFT SIZER SET
- K952184 — CARBOMEDICS SUPRA-ANNULAR VALVE SIZER
- K951368 — CARBOMEDICS EXENDED MITRAL ROTATOR
- K942736 — CARBOMEDICS(R) PROSTHETIC HEART VALVE HOLDER HANDLE
- K934951 — VALVE SIZER
- K842893 — DORR HIP PROSTHESIS, ACETABULAR COMPON
- K842360 — DORR HIP PROSTHESIS FEMORAL COMPONENT
- K833404 — BDH BIPOLAR FEMORAL COMPONENT A3
- K834040 — MINATURE PRESSURE TRANSDUCER
- K833403 — BDH UNIPOLAR FEMORAL COMPONENT A2
- K833468 — BDH UNIVERSAL HIP SYSTEM SURGEON
- K811101 — HYDROXYLAPATITE
- K810382 — HYDROXYLAPATITE ALVEOLAR RIDGE MAIN
- K791416 — PYROLITE CARBON ALVEOLAR MAINTEN IMPLANT
- K791491 — BIOLITE CARBON COATED DENTAL IMPLANT
- K791237 — PYROLITE CARBON ENDOSSEOUS DENTAL IMPL
Data sourced from openFDA. This site is unofficial and independent of the FDA.