Dermapac Inc.
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Dermapac Inc. is a medical device manufacturer, with 178 devices listed in FDA GUDID (FDA Class I) as of 13 Nov 2026.
- Devices
- 178
Registry facts
- Registries
- FDA GUDID 178
- Device classes
- FDA Class I 178
- Identifiers
- DUNS 796088466
What Dermapac Inc. makes
Dermapac Inc. manufactures radiopaque woven surgical sponges, general-purpose surgical sponges, and general surgical procedure kits that are non-medicated and single-use. The company also produces general-purpose absorbent tip applicators or swabs, dental and maxillofacial surgical procedure kits (non-medicated, single-use), instrument management bags, surgical soft-tissue manipulation forceps resembling tweezers (single-use), and umbilical cord tape.
All devices manufactured by Dermapac Inc. are classified as Class I medical devices and are listed in the FDA's Unique Device Identification (FDA UDI) system.
Catalogue
Search and filter all 178 devicesShowing 1-50 of 178
Company details
- DUNS number
- 796088466
- dermapac@msn.com
- Phone
- 203-924-7148
Frequently asked questions
How many devices does Dermapac Inc. have in the registry?
The registry currently lists 178 devices for Dermapac Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermapac Inc.'s devices?
Among its 50 most recently registered devices, Dermapac Inc. has devices listed in FDA GUDID (50 devices).
What risk classes do Dermapac Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Dermapac Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dermapac Inc. in the registry?
The most recently registered devices listed for Dermapac Inc. include Dermapac, Inc. 8926, Dermapac, Inc. 8601, Dermapac, Inc. 9002 and Dermapac, Inc. 1809.