Setmark Inc.
United Statesfrom the FDA registration address FDA FEI 3009688852
Setmark Inc. is a medical device manufacturer, with 42 devices listed in FDA GUDID (FDA Class I and II) as of 15 Nov 2026.
- Devices
- 42
- Registrations
- FDA
- FDA recalls
- 0
Registry facts
- Registries
- FDA GUDID 42
- Device classes
- FDA Class I 37
- FDA Class II 5
- Identifiers
- FDA FEI 3009688852
- DUNS 080798558
At a glance
Market reach
- United States
- FDA FEI
Catalogue
Search and filter all 42 devicesCompany details
- FDA FEI number
- 3009688852
- DUNS number
- 080798558
- Address
- 1712 Pioneer Ave Suite 764, Cheyenne, WY, 82001
Frequently asked questions
How many devices does SETMARK INC. have in the registry?
The registry currently lists 42 devices for SETMARK INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SETMARK INC.'s devices?
Among its 42 most recently registered devices, SETMARK INC. has devices listed in FDA GUDID (42 devices).
What risk classes do SETMARK INC.'s devices fall under?
Among its 42 most recently registered devices, the classes recorded for SETMARK INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from SETMARK INC. in the registry?
The most recently registered devices listed for SETMARK INC. include Setmark Inc. ST-103, Setmark Inc. SS-107, Setmark Inc. SS-100H and Setmark Incorporated TR-135.