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Aretech, LLC

Active in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000008500 FEI 3007797030

Aretech, LLC is a medical device manufacturer based in the United States, with 17 devices listed in FDA GUDID and EUDAMED (FDA Class I; EU Class I) as of 13 Nov 2026.

Devices
17
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 17
  • EUDAMED 3

A device listed in two registries counts in both.

Device classes
  • FDA Class I 14
  • EU Class I 3
Top EMDN categories
Sites and related companies
Identifiers
  • EUDAMED SRN US-MF-000008500
  • FDA FEI 3007797030
  • DUNS 825904738

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI
Authorised rep.
MedEnvoy Global BVNL

What Aretech, LLC makes

Aretech, LLC manufactures gait rehabilitation systems, including electric-powered gait frames and harnesses designed for patient support during mobility training. Their portfolio includes treadmill systems with body-weight support, such as the ZeroG-Lite and Luminaire BWS, as well as specialized harnesses like the Aretech Premium Harness and the BabyG Early Mobilization System for pediatric use.

These devices are classified as Class I under regulatory frameworks and are listed in the EU’s eudamed database and the FDA’s Unique Device Identifier (UDI) system. The company operates from the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue17

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Rows 1-17 of 17

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000008500
FDA FEI number
3007797030
DUNS number
825904738
EUDAMED status
Active
EUDAMED registered name
Aretech, LLC
Registered address
22446, Davis Drive, 20164, Sterling, Virginia, United States
Phone
+1 571 292 8889
PRRC contact
Brendan Gilmore(public in EUDAMED)

Frequently asked questions

How many devices does ARETECH, LLC have in the registry?

The registry currently lists 17 devices for ARETECH, LLC. Devices recorded under merged duplicate company entries are counted once.

Which registries list ARETECH, LLC's devices?

Among its 17 most recently registered devices, ARETECH, LLC has devices listed in EUDAMED (3 devices) and FDA GUDID (17 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do ARETECH, LLC's devices fall under?

Among its 17 most recently registered devices, the classes recorded for ARETECH, LLC's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from ARETECH, LLC in the registry?

The most recently registered devices listed for ARETECH, LLC include Aretech Premium Harness AH-0T, Aretech Premium Harness AH-0S, ZeroG-Lite Treadmill System ZGL-V3 and Aretech Premium Harness AH-0P.

Generated automatically from registry data and not verified by a human reviewer.