Schick Technologies, Inc.: FDA filings under this applicant name
FDA lists 13 510(k) clearances under the applicant name “Schick Technologies, Inc.” (first 1994, latest 2011), across 5 product codes in 2 review panels. Median 510(k) review time under this name: 58 days. Related companies, subsidiaries and acquired businesses that file under other applicant names are counted on their own pages, not here.
510(k) clearances per year
| Year | Clearances | Median review days |
|---|---|---|
| 2012 | 0 | — |
| 2013 | 0 | — |
| 2014 | 0 | — |
| 2015 | 0 | — |
| 2016 | 0 | — |
| 2017 | 0 | — |
| 2018 | 0 | — |
| 2019 | 0 | — |
| 2020 | 0 | — |
| 2021 | 0 | — |
| 2022 | 0 | — |
| 2023 | 0 | — |
| 2024 | 0 | — |
| 2025 | 0 | — |
| 2026 | 0 | — |
Top product codes
| Product code | Device | Submissions | 510(k) clearances |
|---|---|---|---|
| MUH | System, X-Ray, Extraoral Source, Digital | 5 | 5 |
| EAP | Unit, X-Ray, Intraoral | 3 | 3 |
| KGI | Densitometer, Bone | 3 | 3 |
| EIA | Unit, Operative Dental | 1 | 1 |
| MQB | Solid State X-Ray Imager (Flat Panel/Digital Imager) | 1 | 1 |
Review panels
Most recent Schick Technologies, Inc. 510(k) clearances
| 510(k) | Device | Product code | Decision date | Review days |
|---|---|---|---|---|
| K110768 | COMPUTED DENTAL RADIOGRAPHY | MUH | 2011-04-20 | 33 |
| K093453 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | EAP | 2009-11-30 | 25 |
| K072134 | SCHICK COMPUTED ORAL RADIOLOGY SYSTEM | MUH | 2007-11-02 | 92 |
| K053558 | CEPH, MODEL 4900 | MUH | 2006-02-17 | 58 |
| K041385 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | EAP | 2004-06-07 | 13 |
| K031291 | CDR PANX, MODEL 4792 | MUH | 2003-05-05 | 12 |
| K022953 | MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM | MUH | 2002-10-02 | 27 |
| K001429 | MODIFICATION TO ACCUDEXA BONE DENSITOMETER | KGI | 2000-05-26 | 21 |
| K982661 | CDR - PAN MODEL 4700 | MQB | 1998-12-11 | 134 |
| K981124 | ACCUDEXA BONE DENSITOMETER | KGI | 1998-06-04 | 69 |
3 earlier clearances. See the full list in Caduvo.
Recalls
openFDA lists no recalls under a recalling firm named Schick Technologies, Inc..
Recalling firms are matched to this applicant name by name only (same normalization), so related entities that recall under another name are not counted. A recall count says nothing about how safe one company's devices are compared with another's.
Frequently asked questions
How many FDA 510(k) clearances are listed under Schick Technologies, Inc.?
FDA lists 13 510(k) clearances under the applicant name “Schick Technologies, Inc.” (first 1994, latest 2011), across 5 product codes in 2 review panels. Filings under other applicant names, such as subsidiaries, are not included.
How long has FDA taken to clear 510(k)s filed by Schick Technologies, Inc.?
The median time from FDA receipt to decision across 510(k)s cleared under the name Schick Technologies, Inc. is 58 days.
Which FDA product codes appear under Schick Technologies, Inc.?
The most frequent FDA product codes under this applicant name are MUH (System, X-Ray, Extraoral Source, Digital, 5); EAP (Unit, X-Ray, Intraoral, 3); KGI (Densitometer, Bone, 3).
Next steps
- See all 13 Schick Technologies, Inc. clearances with predicates and recalls
- Run predicate analysis for product code MUH, Schick Technologies, Inc.'s most frequent
Data from openFDA (510(k), PMA, De Novo, device recalls), ClinicalTrials.gov and SEC company tickers. Each page covers one FDA applicant name, with punctuation and legal suffixes removed; filings under other names are not included. Review days run from FDA receipt to decision. Not regulatory advice. Report an error in this data.