Schick Technologies, Inc.
Long Island City, NY, US
Schick Technologies, Inc. appears in FDA device records in Long Island City, NY. FDA records list 13 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 13
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 13 510(k) clearances for Schick Technologies, Inc. between 1994 and 2011. The busiest year on record is 1998, with 2. The most recent is 2011, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1994 | 1 |
| 1996 | 1 |
| 1997 | 1 |
| 1998 | 2 |
| 2000 | 1 |
| 2002 | 1 |
| 2003 | 1 |
| 2004 | 1 |
| 2006 | 1 |
| 2007 | 1 |
| 2009 | 1 |
| 2011 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K110768 | COMPUTED DENTAL RADIOGRAPHY | MUH | Substantially Equivalent | |
| K093453 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | EAP | Substantially Equivalent | |
| K072134 | SCHICK COMPUTED ORAL RADIOLOGY SYSTEM | MUH | Substantially Equivalent | |
| K053558 | CEPH, MODEL 4900 | MUH | Substantially Equivalent | |
| K041385 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | EAP | Substantially Equivalent | |
| K031291 | CDR PANX, MODEL 4792 | MUH | Substantially Equivalent | |
| K022953 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | MUH | Substantially Equivalent | |
| K001429 | MODIFICATION TO ACCUDEXA BONE DENSITOMETER | KGI | Substantially Equivalent | |
| K982661 | CDR - PAN MODEL 4700 | MQB | Substantially Equivalent | |
| K981124 | ACCUDEXA BONE DENSITOMETER | KGI | Substantially Equivalent | |
| K971735 | ACCUDEXA BONE DENSITOMETER | KGI | Substantially Equivalent | |
| K963778 | CDR-CAM | EIA | Substantially Equivalent | |
| K933455 | COMPUTED ORAL RADIOLOGY SYSTEM | EAP | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain