Orthocor Medical Inc.
Also registered as Orthocor Medical
Country not established FDA establishment FEI 3008216220
- Devices
- 3
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
- 510(k) 510(k)
Orthocor Knee System Basic Ref K091996
510(k) 510(k)Orthocor Knee System, Median, Large, X-Large Ref K092044
510(k) 510(k)
Company details
- FDA FEI number
- 3008216220
- Address
- 8611 W 35W Service Dr. NE, Blaine, MN, 55449
Frequently asked questions
How many devices does ORTHOCOR MEDICAL INC. have in the registry?
The registry currently lists 3 devices for ORTHOCOR MEDICAL INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list ORTHOCOR MEDICAL INC.'s devices?
Among its 3 most recently registered devices, ORTHOCOR MEDICAL INC. has devices listed in FDA 510(k) (3 devices).
What risk classes do ORTHOCOR MEDICAL INC.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for ORTHOCOR MEDICAL INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ORTHOCOR MEDICAL INC. in the registry?
The most recently registered devices listed for ORTHOCOR MEDICAL INC. include ORTHOCOR ACTIVE DEVICE ORTHOCOR GENERAL USE ACTIVE DEVICE, ORTHOCOR KNEE SYSTEM BASIC and ORTHOCOR KNEE SYSTEM, MEDIAN, LARGE, X-LARGE.