The following data is part of a premarket notification filed by Titan Implants, Inc. with the FDA for Titan Dental Implant System.
| Device ID | K042971 | 
| 510k Number | K042971 | 
| Device Name: | TITAN DENTAL IMPLANT SYSTEM | 
| Classification | Implant, Endosseous, Root-form | 
| Applicant | TITAN IMPLANTS, INC. 4329 GRAYDON ROAD San Diego, CA 92130 | 
| Contact | Floyd G Larson | 
| Correspondent | Floyd G Larson TITAN IMPLANTS, INC. 4329 GRAYDON ROAD San Diego, CA 92130  | 
| Product Code | DZE | 
| CFR Regulation Number | 872.3640 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2004-10-28 | 
| Decision Date | 2005-01-14 | 
| Summary: | summary |