Not currently registered with FDA under this name
Doctor'S Research Group, Inc.
Wolcott, CT, United States. Named as applicant on 4 dental 510(k) clearances between 1998 and 1999. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 41998–1999
- Markets registered in
- 418 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 1990–2026
Registered in 4 markets
Where regulators' registries name Doctor'S Research Group, Inc. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Applicant | Doctor'S Research Group, Inc. | 4 clearances | 1998–1999 | Below |
| Canada | Health Canada | Registration holder | DOCTORS RESEARCH GROUP INC | 14 | 1999–2007 | Pure Global AI |
| Colombia | INVIMA | Manufacturer | DOCTORS RESEARCH GROUP. INC | 3 | — | Pure Global AI |
| Israel | AMAR | Manufacturer | Doctors Research Group Inc. | 1 | — | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
510(k) clearances
Clearances on which FDA names Doctor'S Research Group, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 14 Sep 1999 | K990212 | LOCKJAW 15 MINUTE INTERMAXILLARY FIXATION SYSTEM,MODEL LJ100-00 | DYX Intraoral Wire Lock and Ligature |
| 10 Jun 1999 | K990920 | DRG TITANIUM BONE PLATE | JEY Bone Plate |
| 2 Dec 1998 | K981881 | DRG SHERLOCK MF BONE SCREW, COCRMO SELF-TAPPING, TI ALLOY SELF-TAPPING/SELF DRILLING, COCRMO SELF-TAPPING/ SELF DRILLING | DZL Intraosseous Fixation Screw |
| 13 Mar 1998 | K974817 | DRG MF TITANIUN ALLOY BONE SCREW 1.0MM, 1.2MM, 1.3MM, 1.5MM, 1.7MM, 2.0MM, 2.4MM | DZL Intraosseous Fixation Screw |
Sources
FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record of the most recent filing, which can be a US agent.