Schick Technologies, Inc.
Schick Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2011.
Top product codes for Schick Technologies, Inc.
Recent clearances by Schick Technologies, Inc.
- K110768 — COMPUTED DENTAL RADIOGRAPHY
- K093453 — MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
- K072134 — SCHICK COMPUTED ORAL RADIOLOGY SYSTEM
- K053558 — CEPH, MODEL 4900
- K041385 — MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
- K031291 — CDR PANX, MODEL 4792
- K022953 — MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
- K001429 — MODIFICATION TO ACCUDEXA BONE DENSITOMETER
- K982661 — CDR - PAN MODEL 4700
- K981124 — ACCUDEXA BONE DENSITOMETER
- K971735 — ACCUDEXA BONE DENSITOMETER
- K963778 — CDR-CAM
- K933455 — COMPUTED ORAL RADIOLOGY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.