Midwest Rf, LLC
United StatesFDA applicant, unverified
- Devices
- 9
What Midwest Rf, LLC makes
Midwest RF, LLC manufactures medical positioning and stimulation devices, including pediatric and adult patient positioners for surgical and diagnostic procedures, as well as brain coils and arrays for MRI-guided deep brain stimulation (DBS) and neurostimulation. Their portfolio also includes a hair growth stimulation system and specialized coils for head and neck imaging. These products are designed for use in clinical and procedural settings requiring precise patient alignment or neuromodulation.
The company’s devices are classified under FDA Class II, requiring premarket notification (510(k)) clearance. Their products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Model 1300GE-64: Pediatric Positioner Ref K030317
Regimes: 510(k) Registry: 510(k)Sv Dbs Brain Array, Model 1500SV-SMS64 Ref K090267
Regimes: 510(k) Registry: 510(k)Sv Dbs Vrain Array Ref K111259
Regimes: 510(k) Registry: 510(k)Special Procedures Head Coil; Model # 1100GE-64 Ref K003386
Regimes: 510(k) Registry: 510(k)Brain Coil, Model 9800GE-64 Ref K003097
Regimes: 510(k) Registry: 510(k)Mep-90 Hair Growth Stimulation System Ref K091496
Regimes: 510(k) Registry: 510(k)Model 6900GE-64: C-Spine Array Ref K002860
Regimes: 510(k) Registry: 510(k)Special Procedures Ii Head Coil, Model 1400GE-64 Ref K051618
Regimes: 510(k) Registry: 510(k)Model 6600GE-64: Trama Neck Array Ref K002864
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Midwest Rf, LLC have in the registry?
The registry currently lists 9 devices for Midwest Rf, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Midwest Rf, LLC's devices?
Among its 9 most recently registered devices, Midwest Rf, LLC has devices listed in FDA 510(k) (9 devices).
What risk classes do Midwest Rf, LLC's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Midwest Rf, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Midwest Rf, LLC in the registry?
The most recently registered devices listed for Midwest Rf, LLC include MODEL 1300GE-64: PEDIATRIC POSITIONER, SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64, SV DBS VRAIN ARRAY and SPECIAL PROCEDURES HEAD COIL; MODEL # 1100GE-64.