Engineered Orthopedic Technologies, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Engineered Orthopedic Technologies, Inc. makes
Engineered Orthopedic Technologies, Inc. manufactures specialized medical devices for neurosurgical and orthopedic applications, including the MALCOLM-LYNN™ EOT Suction Regulator Valve (SRV) for controlled fluid management and the MALCOLM-RAND Microneurosurgical Cranio-Xray Frame for stabilizing cranial procedures.
The company’s portfolio consists of Class II devices, each authorised via FDA 510(k) clearance. These products are listed under the FDA’s regulatory framework and are intended for use in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Engineered Orthopedic Technologies, Inc. have in the registry?
The registry currently lists 2 devices for Engineered Orthopedic Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Engineered Orthopedic Technologies, Inc.'s devices?
Among its 2 most recently registered devices, Engineered Orthopedic Technologies, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Engineered Orthopedic Technologies, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Engineered Orthopedic Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Engineered Orthopedic Technologies, Inc. in the registry?
The most recently registered devices listed for Engineered Orthopedic Technologies, Inc. include MALCOLM-LYNN(TM) EOT SUCTION REG VALVE(TM) (SRV) ) and MALCOLM-RAND MICRONEUROSURGICAL CRANIO-XRAY FRAME.