The following data is part of a premarket notification filed by Implant Integration Systems, Inc. with the FDA for Dual Integrator Dental Implant.
| Device ID | K944225 |
| 510k Number | K944225 |
| Device Name: | DUAL INTEGRATOR DENTAL IMPLANT |
| Classification | Implant, Endosseous, Root-form |
| Applicant | IMPLANT INTEGRATION SYSTEMS, INC. 6161 CLARK RD., STE. 8 Paradise, CA 95969 |
| Contact | Fred N Hanosh |
| Correspondent | Fred N Hanosh IMPLANT INTEGRATION SYSTEMS, INC. 6161 CLARK RD., STE. 8 Paradise, CA 95969 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1994-08-30 |
| Decision Date | 1995-09-27 |