Postmeds, Inc.
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Postmeds, Inc. is a medical device manufacturer, with 2 devices listed in FDA GUDID (FDA Class I) as of 14 Nov 2026.
- Devices
- 2
Registry facts
- Registries
- FDA GUDID 2
- Device classes
- FDA Class I 2
- Identifiers
- DUNS 080974592
What Postmeds, Inc. makes
Postmeds, Inc. manufactures capillary blood collection sets designed for home use, as well as non-insulated specimen container mailers for transporting biological samples. Their portfolio also includes in vitro diagnostic (IVD) specimen stabilization reagents, which preserve sample integrity during testing.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company operates within the United States, adhering to applicable domestic regulatory requirements for medical devices.
Catalogue
- Registry: GUDID
- Registry: GUDID
Company details
- DUNS number
- 080974592
Frequently asked questions
How many devices does Postmeds, Inc. have in the registry?
The registry currently lists 2 devices for Postmeds, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Postmeds, Inc.'s devices?
Among its 2 most recently registered devices, Postmeds, Inc. has devices listed in FDA GUDID (2 devices).
What risk classes do Postmeds, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Postmeds, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Postmeds, Inc. in the registry?
The most recently registered devices listed for Postmeds, Inc. include Truepill Inc. 1.