# ActiGraph

> Medical device manufacturer record on deviCERTS, compiled from public registries. ActiGraph is a medical device manufacturer based in the United States, with 7 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (EU Class I; FDA Class II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/actigraph>
- Also registered as: Actigraph, LLC
- Country: United States (from SRN)
- EUDAMED actor status: active
- Role: Manufacturer
- Registrations: EUDAMED
- EUDAMED SRN: US-MF-000007954

## Figures

- Devices: 7
- 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: EUDAMED 4, FDA GUDID 4, FDA 510(k) 3
- Device classes: EU Class I 4, FDA Class II 3
- EMDN [V90 Various devices not included in other classes](https://devicerts.com/categories/emdn/V90): 4 devices

## Sites and related companies

- Authorised representative: [Emergo Europe B.V.](https://devicerts.com/representatives/emergo-europe-bv-nl-ar-000000116) (Netherlands)

## Devices

The first 7 of 7, in the order of the canonical page, which lists them all.

- [ActiGraph CentrePoint Insight Watch](https://devicerts.com/devices/actigraph-centrepoint-insight-watch-lel) · ref K181077 · Class II · 510(k) · status: Active · decision 2018-05-24
- [Actitrainer](https://devicerts.com/devices/actitrainer-isd) · ref K080545 · Class II · 510(k) · status: Active · decision 2008-07-24
- [ActiGraph LEAP activity monitor (ActiGraph LEAP)](https://devicerts.com/devices/actigraph-leap-activity-monitor-actigraph-leap-lel) · ref K231532 · Class II · 510(k) · status: Active · decision 2023-06-23
- [ActiGraph wGT3X-BT](https://devicerts.com/devices/actigraph-wgt3x-bt-wgt3x-bt) · Class I · EUDAMED, GUDID · status: Active
- [ActiGraph LEAP](https://devicerts.com/devices/actigraph-leap-leap) · Class I · EUDAMED, GUDID · status: Active
- [ActiGraph GT9X](https://devicerts.com/devices/actigraph-gt9x-gt9x) · Class I · EUDAMED, GUDID · status: Active
- [ActiGraph CPW01](https://devicerts.com/devices/actigraph-cpw01-cpw01) · Class I · EUDAMED, GUDID · status: Active

## Source and citation

- Cite as: ActiGraph. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/actigraph (data as of 2026-11-15).
- Data sources: [EUDAMED](https://ec.europa.eu/tools/eudamed), [FDA GUDID](https://accessgudid.nlm.nih.gov/), [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- EUDAMED record synced: 2026-11-07
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/actigraph.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/actigraph
- 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.