# Dymedso, Inc.

> Medical device manufacturer record on deviCERTS, compiled from public registries. Dymedso, Inc. is a medical device manufacturer, with 6 devices listed in FDA 510(k) and FDA GUDID (FDA Class II) as of 15 Nov 2026.

- Canonical page: <https://devicerts.com/manufacturers/dymedso-inc>
- Country: United States (FDA applicant, unverified)
- Role: Manufacturer
- DUNS: 243498438

## Figures

- Devices: 6
- 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, FDA GUDID 3
- Device classes: FDA Class II 6

## Devices

The first 6 of 6, in the order of the canonical page, which lists them all.

- [Frequencer V2.3](https://devicerts.com/devices/frequencer-dymv2-3-945fdb14) · Class II · GUDID · status: Active
- [Frequencer V2.3](https://devicerts.com/devices/frequencer-dymv2-3) · Class II · GUDID · status: Active
- [Frequencer V2X](https://devicerts.com/devices/frequencer-dymv2x) · Class II · GUDID · status: Active
- [Frequencer Model V2X](https://devicerts.com/devices/frequencer-model-v2x-byi) · ref K100749 · Class II · 510(k) · status: Active · decision 2010-08-31
- [Frequencer](https://devicerts.com/devices/frequencer-byi) · ref K103176 · Class II · 510(k) · status: Active · decision 2011-01-26
- [Frequencer, Model 1001](https://devicerts.com/devices/frequencer-model-1001-byi) · ref K063645 · Class II · 510(k) · status: Active · decision 2007-03-15

## Source and citation

- Cite as: Dymedso, Inc. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/dymedso-inc (data as of 2026-11-15).
- Data sources: [FDA 510(k)](https://open.fda.gov/apis/device/510k/), [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/dymedso-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/dymedso-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.