Dymedso, Inc.
United StatesFDA applicant, unverified
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.
- Devices
- 6
Registry facts
- Registries
- FDA 510(k) 3
- FDA GUDID 3
- Device classes
- FDA Class II 6
- Identifiers
- DUNS 243498438
What Dymedso, Inc. makes
Dymedso, Inc. manufactures chest-percussion airway secretion-clearing systems designed to assist patients in clearing respiratory secretions. The devices are primarily used for managing conditions that cause mucus buildup in the airways, such as chronic obstructive pulmonary disease (COPD) or cystic fibrosis.
The company’s products are classified as Class II medical devices under FDA regulations and are authorised through the 510(k) and UDI pathways.
Catalogue
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
Frequencer Model V2X Ref K100749
Regimes: 510(k) Registry: 510(k)Frequencer Ref K103176
Regimes: 510(k) Registry: 510(k)Frequencer, Model 1001 Ref K063645
Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 243498438
Frequently asked questions
How many devices does Dymedso, Inc. have in the registry?
The registry currently lists 6 devices for Dymedso, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dymedso, Inc.'s devices?
Among its 6 most recently registered devices, Dymedso, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Dymedso, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Dymedso, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dymedso, Inc. in the registry?
The most recently registered devices listed for Dymedso, Inc. include FREQUENCER V2.3, FREQUENCER V2X, FREQUENCER MODEL V2X and FREQUENCER.