Doctor'S Research Group, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 14
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What Doctor'S Research Group, Inc. makes
Doctor'S Research Group, Inc. manufactures orthopedic fixation devices, including titanium bone plates, threaded bone screws in various sizes and alloys, and bone cement for surgical applications. Their portfolio also includes medical imaging tools like stethoscopes with antimicrobial properties, as well as laryngeal augmentation implants and suture anchors for soft tissue stabilization.
The company’s devices are classified under Class II regulatory standards in the United States and are listed via 510(k) clearance through the FDA. The manufacturer operates within the US regulatory framework, adhering to requirements for medical devices in orthopedics, diagnostics, and surgical implants.
Catalogue
Search and filter all 14 devicesFDA recalls
FDA recall records list 1 recall initiated by Doctor'S Research Group, Inc., initiated on 2012-04-06. By recorded status: 1 terminated. The reasons filed fall into these groups: manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2012
- 6 Apr 2012 Z-1496-2012 Not yet classified Terminated Bone cement strength and stiffness fall below specification at body temperature
Frequently asked questions
How many devices does Doctor'S Research Group, Inc. have in the registry?
The registry currently lists 14 devices for Doctor'S Research Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Doctor'S Research Group, Inc.'s devices?
Among its 14 most recently registered devices, Doctor'S Research Group, Inc. has devices listed in FDA 510(k) (14 devices).
What risk classes do Doctor'S Research Group, Inc.'s devices fall under?
Among its 14 most recently registered devices, the classes recorded for Doctor'S Research Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Doctor'S Research Group, Inc.?
FDA recall records list 1 recall initiated by Doctor'S Research Group, Inc., the most recent initiated on 2012-04-06. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Doctor'S Research Group, Inc. in the registry?
The most recently registered devices listed for Doctor'S Research Group, Inc. include DRG REACTION CHAMBER/SAFETY TIP, DRG TITANIUM BONE PLATE, DRG ORTHOHEX SS BONE SCREW and KRYPTONITE BONE CEMENT.