Identity
- Trade Name
- AcroGrip™ Device FDA UDI
- Generic Name
- Hand dynamometer/pinchmeter, electronic FDA UDI
- Device Name
- Hand dynamometer intended for use with the AcroVal™ Neurosensory & Motor Testing System (NSMTS) to measure grasp strength. FDA UDI
- Model / Reference
- EN-247 FDA UDI
- Description
- Hand dynamometer intended for use with the AcroVal™ Neurosensory & Motor Testing System (NSMTS) to measure grasp strength. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10850828007012 FDA UDI
- 510(k) Number
- K923963 FDA UDI
- FDA Product Code
- LBB FDA UDI
- GMDN Term
- Hand dynamometer/pinchmeter, 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Hand dynamometer/pinchmeter, electronic
AcroGrip™ Device by AxoGen Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hand dynamometer/pinchmeter, electronic.
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- Biometrics Ltd Dynamometer — BIOMETRICS LIMITED · Class II
- microFET Pinch — Hoggan Scientific L.L.C. · Class II
- Eforto — Uniweb · Class II
- Northstar Echo Grip Gauge — J-Tech Medical, Inc. · Class I
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
- AxoGen Corporation
Sources (1)
- FDA UDI b74eaf51-e11e-45c2-a85d-c63d0060678e 35 fields · synced Jun 6, 2026