I-Rep, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 8
Catalogue
Rotagym Ref K832940
510(k) 510(k)Accutrac Traction Unit Ref K930691
510(k) 510(k)Adjustable Treatment Tables Ref K851690
510(k) 510(k)Latham Table Ref K930692
510(k) 510(k)Physical Medicine & Rehabilitation Equip Ref K822906
510(k) 510(k)Rehabilitation Tables Ref K854947
510(k) 510(k)Medtron Type P-300 Ultrasonic Therapy Unit Ref K861864
510(k) 510(k)Vacupulse Vacuum Unit Ref K842268
510(k) 510(k)
Frequently asked questions
How many devices does I-Rep, Inc. have in the registry?
The registry currently lists 8 devices for I-Rep, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list I-Rep, Inc.'s devices?
Among its 8 most recently registered devices, I-Rep, Inc. has devices listed in FDA 510(k) (8 devices).
What risk classes do I-Rep, Inc.'s devices fall under?
Among its 8 most recently registered devices, the classes recorded for I-Rep, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from I-Rep, Inc. in the registry?
The most recently registered devices listed for I-Rep, Inc. include ROTAGYM, ACCUTRAC TRACTION UNIT, ADJUSTABLE TREATMENT TABLES and LATHAM TABLE.