Identity
- Trade Name
- microfet2 FDA UDI
- Generic Name
- Dynamometer force gauge FDA UDI
- Device Name
- microFET®2 is a hand-held dynamometer (HHD) for performing muscle tests to quantitatively measure muscle weakness caused by injury, as well as measure general muscle strength. The device is used to convey an individual’s ability to resist force for a specific muscle or muscle group being tested. FDA UDI
- Model / Reference
- 5021 FDA UDI
- Description
- microFET®2 is a hand-held dynamometer (HHD) for performing muscle tests to quantitatively measure muscle weakness caused by injury, as well as measure general muscle strength. The device is used to convey an individual’s ability to resist force for a specific muscle or muscle group being tested. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850002429008 FDA UDI
- 510(k) Number
- K162412 FDA UDI
- FDA Product Code
- LBB FDA UDI
- GMDN Term
- Dynamometer force gauge 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Dynamometer force gauge
microfet2 by Hoggan Scientific L.L.C. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 |
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Manufacturer
- Manufacturer
- Hoggan Scientific L.L.C.
Sources (1)
- FDA UDI 8877a812-0bd7-42b9-8318-6bb8185e7381 34 fields · synced Jun 1, 2026