ActivForce 2
Wireless digital dynamometer and goniometer.
2manufacturers in China registered for this device type
1catalogue number
2recalls on this code
Who Else Makes It
All of them in Guangdong. 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Suga Electronics (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 3 |
| Suga Technology (Dongguan) Co.. Ltd. | Dongguan | Guangdong | Contract manufacturer | 2 |
Record
| Listed by | Activbody, United States |
|---|---|
| FDA product code | LBB |
| Device type | Dynamometer, Ac-Powered |
| Device class | Class 2 |
| Regulation | 21 CFR 888.1240 |
| Establishment | Specification developer, Complaint-file establishment, Manufacturer |
| Premarket notification | Exempt |
| Record published | 2025-09-03 |
| Record revised | 2026-03-11 (version 2) |
Specifications
| MRI safety | MR Unsafe |
|---|---|
| Label carries | manufacturing date, serial number |
| Distribution end date | 2032-12-31 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| Activ5-M | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Kinvent | Kinvent Hellas | 4 |
| SR-3053 | RED OAK Instruments, LLC | 2 |
| Innobyte Full-Arch Mouthpiece Sensor | Kube Innovation Inc. | 1 |
| KForce Bubble | Kinvent Biomecanique | 1 |
| Innobyte Clinical Package | Kube Innovation Inc. | 1 |
| AcroPinch™ Device | Axogen Corporation | 1 |
| microFET Pinch | Hoggan Scientific L.L.C. | 1 |
| Innobyte Bilateral Mouthpiece Replacement | Kube Innovation Inc. | 1 |
| microfet2 | Hoggan Scientific L.L.C. | 1 |
| Eforto | UniWeb BV | 1 |
| KForce Muscle Controller | Kinvent Biomecanique | 1 |
| microfet3 | Hoggan Scientific L.L.C. | 1 |
Showing 12 of 19. All products under Dynamometer, Ac-Powered
Recalls
2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity |
|---|---|---|---|---|
| 2021-11-30 | Class II | Other | Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing to register and list its medical devices with U.S. Food and Drug Administration | 501 kits |
| 2021-11-30 | Class II | Other | Due to: 1) Manufacturing issue that result in inaccurate force measurement which may lead to may potential lead to incorrect treatment planning. 2) Firm failing to register and list its medical devices with U.S. Food and Drug Administration | 145 kits in U.S. |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.