# Bionik, Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Bionik, Inc. is a medical device manufacturer, with 2 devices listed in FDA GUDID (FDA Class I and II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/bionik-inc>
- Country: not established
- Role: Manufacturer
- DUNS: 080397777

## Figures

- Devices: 2
- FDA recalls (matched to the firm by name): 0

## Registry facts

*Every device of the manufacturer. A device listed in two registries counts in both.*

- Registries: FDA GUDID 2
- Device classes: FDA Class I 1, FDA Class II 1

## Devices

The first 2 of 2, in the order of the canonical page, which lists them all.

- [InMotion ARM SE4](https://devicerts.com/devices/inmotion-arm-se4) · Class I · GUDID · status: Listed
- [InMotion ARM/HAND SE4HA4](https://devicerts.com/devices/inmotion-arm-hand-se4ha4) · Class II · GUDID · status: Listed

## Source and citation

- Cite as: Bionik, Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/bionik-inc (data as of 2026-11-15).
- Data sources: [FDA GUDID](https://accessgudid.nlm.nih.gov/)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/bionik-inc.json>
- Licence: [CC BY 4.0](https://creativecommons.org/licenses/by/4.0/). The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.
- Attribution: DevicErts, https://devicerts.com/manufacturers/bionik-inc
- Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails.