Dolphin Medical Technologies, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 2
What Dolphin Medical Technologies, Inc. makes
Dolphin Medical Technologies, Inc. manufactures orthopedic screw systems, including the DRG Medium Screw System and the DRG Large Screw System, designed for spinal fixation and stabilization procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Drg Medium Screw System Ref K990019
510(k) 510(k)Drg Large Screw System Ref K973810
510(k) 510(k)
Frequently asked questions
How many devices does Dolphin Medical Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Dolphin Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dolphin Medical Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Dolphin Medical Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dolphin Medical Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dolphin Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dolphin Medical Technologies, Inc. in the registry?
The most recently registered devices listed for Dolphin Medical Technologies, Inc. include DRG MEDIUM SCREW SYSTEM and DRG LARGE SCREW SYSTEM.