Identity
- Trade Name
- KINVENT FDA UDI
- Generic Name
- Back/leg/chest dynamometer, electronic FDA UDI
- Device Name
- Muscle Controller is a hand held dynamometer used for the evaluation of muscles strength. You can assess isometric strength by the way of the peak force as well as of the average force for a specific muscle or muscle groups.The Muscle Controller allows to quantitatively measure the muscle strength and the deficit percentage caused by injury compared to the strength of the healthy side FDA UDI
- Model / Reference
- Muscle Controller V2R01 FDA UDI
- Description
- Muscle Controller is a hand held dynamometer used for the evaluation of muscles strength. You can assess isometric strength by the way of the peak force as well as of the average force for a specific muscle or muscle groups.The Muscle Controller allows to quantitatively measure the muscle strength and the deficit percentage caused by injury compared to the strength of the healthy side FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03770011995103 FDA UDI
- FDA Product Code
- LBB FDA UDI
- GMDN Term
- Back/leg/chest dynamometer, electronic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1240 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Back/leg/chest dynamometer, electronic
Kinvent by Kinvent Hellas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Back/leg/chest dynamometer, electronic.
- Lafayette Hand-Held Dynamometer — Lafayette Instrument Company · Class I
- ActivForce 2 — ACTIVBODY · Class II
- KINVENT — KINVENT HELLAS · Class II
- KINVENT — KINVENT HELLAS · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Kinvent Hellas
Sources (1)
- FDA UDI 57fc7200-4569-44a9-9830-b03873199989 35 fields · synced Jun 8, 2026