# Team Technologies, Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Team Technologies, Inc. is a medical device manufacturer, with 3 devices listed in FDA 510(k) (FDA Class I and II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/team-technologies-inc>
- Country: United States (FDA applicant, unverified)
- Role: Manufacturer
- DUNS: 078550672

## Figures

- Devices: 3
- 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 510(k) 3
- Device classes: FDA Class I 2, FDA Class II 1

## Devices

The first 3 of 3, in the order of the canonical page, which lists them all.

- [Disposable Prophylaxis Angle](https://devicerts.com/devices/disposable-prophylaxis-angle-egs) · ref K941189 · Class I · 510(k) · status: Active · decision 1994-05-16
- [Cytology Brush](https://devicerts.com/devices/cytology-brush-hht) · ref K971849 · Class II · 510(k) · status: Active · decision 1997-07-24
- [Extended Straight Attachment](https://devicerts.com/devices/extended-straight-attachment-egs) · ref K994024 · Class I · 510(k) · status: Active · decision 2000-02-03

## Source and citation

- Cite as: Team Technologies, Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/team-technologies-inc (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/)
- FDA recall data as of: 2026-11-01
- Data as of: 2026-11-15
- JSON: <https://devicerts.com/manufacturers/team-technologies-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/team-technologies-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.