The following data is part of a premarket notification filed by Dentalez, Inc. with the FDA for Concenpiece,high-speed Handpiece Series.
| Device ID | K113301 |
| 510k Number | K113301 |
| Device Name: | CONCENPIECE,HIGH-SPEED HANDPIECE SERIES |
| Classification | Handpiece, Air-powered, Dental |
| Applicant | DENTALEZ, INC. 1816 COLONIAL VILLAGE LN. Lancaster, PA 17601 |
| Contact | Jim Watkins |
| Correspondent | Jim Watkins DENTALEZ, INC. 1816 COLONIAL VILLAGE LN. Lancaster, PA 17601 |
| Product Code | EFB |
| CFR Regulation Number | 872.4200 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-11-08 |
| Decision Date | 2012-01-23 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| D7022656340 | K113301 | 000 |
| D7022656300 | K113301 | 000 |