# TENTECH Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries.

- Canonical page: <https://devicerts.com/manufacturers/tentech-inc>
- Country: not established
- Role: Manufacturer
- Registrations: FDA
- FDA FEI: 3025606176
- DUNS: 693713346

## Figures

- Devices: none on record
- FDA recalls (matched to the firm by name): 0
- FDA establishments: 1

## Sites and related companies

- Authorised representative: [Javitech Consulting GmbH](https://devicerts.com/representatives/javitech-consulting-gmbh-de-ar-000045915) (Germany)

## Devices

No device on record.

## Source and citation

- Cite as: TENTECH Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/tentech-inc (data as of 2026-11-14).
- Data sources: [FDA registration and listing](https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-14
- JSON: <https://devicerts.com/manufacturers/tentech-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/tentech-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.