The following data is part of a premarket notification filed by Ultradent Products, Inc. with the FDA for File-eze.
| Device ID | K934415 |
| 510k Number | K934415 |
| Device Name: | FILE-EZE |
| Classification | Cleanser, Root Canal |
| Applicant | ULTRADENT PRODUCTS, INC. 2057 SUMMIT DR. Lake Oswego, OR 97034 |
| Contact | Arthur J Saffir |
| Correspondent | Arthur J Saffir ULTRADENT PRODUCTS, INC. 2057 SUMMIT DR. Lake Oswego, OR 97034 |
| Product Code | KJJ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-09-10 |
| Decision Date | 1994-04-13 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00883205106711 | K934415 | 000 |
| 00883205105431 | K934415 | 000 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FILE-EZE 74237678 1714978 Live/Registered |
Ultradent Products, Inc. 1992-01-14 |