Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Schick Technologies, Inc. — Predicate Candidate Screening
13 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
58 daysmedian FDA review time
201 days90th percentile
13clearances measured
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K110768 | COMPUTED DENTAL RADIOGRAPHY | Schick Technologies, Inc. | 2011-04-20 | 33 | 0 |
| K093453 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | Schick Technologies, Inc. | 2009-11-30 | 25 | 0 |
| K072134 | SCHICK COMPUTED ORAL RADIOLOGY SYSTEM | Schick Technologies, Inc. | 2007-11-02 | 92 | 0 |
| K053558 | CEPH, MODEL 4900 | Schick Technologies, Inc. | 2006-02-17 | 58 | 0 |
| K041385 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | Schick Technologies, Inc. | 2004-06-07 | 13 | 0 |
| K031291 | CDR PANX, MODEL 4792 | Schick Technologies, Inc. | 2003-05-05 | 12 | 0 |
| K022953 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | Schick Technologies, Inc. | 2002-10-02 | 27 | 0 |
| K001429 | MODIFICATION TO ACCUDEXA BONE DENSITOMETER | Schick Technologies, Inc. | 2000-05-26 | 21 | 0 |
| K982661 | CDR - PAN MODEL 4700 | Schick Technologies, Inc. | 1998-12-11 | 134 | 0 |
| K981124 | ACCUDEXA BONE DENSITOMETER | Schick Technologies, Inc. | 1998-06-04 | 69 | 0 |
| K971735 | ACCUDEXA BONE DENSITOMETER | Schick Technologies, Inc. | 1997-12-02 | 204 | 0 |
| K963778 | CDR-CAM | Schick Technologies, Inc. | 1996-11-22 | 63 | 0 |
| K933455 | COMPUTED ORAL RADIOLOGY SYSTEM | Schick Technologies, Inc. | 1994-01-31 | 201 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda