Skip to content

Marpac, Inc.

United StatesFDA applicant, unverified FDA FEI 1000117278

Marpac, Inc. is a medical device manufacturer, with 41 devices listed in FDA GUDID and FDA 510(k) (FDA Class I and II) as of 13 Nov 2026.

Devices
41
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 38
  • FDA 510(k) 3

A device listed in two registries counts in both.

Device classes
  • FDA Class I 38
  • FDA Class II 3
Identifiers
  • FDA FEI 1000117278
  • DUNS 794035683

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Marpac, Inc. makes

Marpac, Inc. manufactures single-use medical devices for airway management and patient stabilization, including tracheostomy tube neck holders, endotracheal tube holders, and CPAP/BPAP chin straps. Their portfolio also includes non-silicone dressing-fixation skin adhesive tape and reusable anesthesia mask straps. The company produces urinary catheter holders to secure catheters in place during patient care.

The company’s devices are regulated under FDA classifications, with products falling into Class I and Class II categories. These devices are listed in the FDA’s 510(k) and UDI registries, ensuring compliance with U.S. medical device regulations.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue41

Newest first, rows 1-41 of 41

Search and filter all 41 devices
Skip device list

Rows 1-41 of 41

Company details

FDA FEI number
1000117278
DUNS number
794035683
Address
4801 Lincoln Rd NE, ALBUQUERQUE, NM, 87109
Phone
1-505-344-4740

Frequently asked questions

How many devices does Marpac, Inc. have in the registry?

The registry currently lists 41 devices for Marpac, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Marpac, Inc.'s devices?

Among its 41 most recently registered devices, Marpac, Inc. has devices listed in FDA 510(k) (3 devices) and FDA GUDID (38 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Marpac, Inc.'s devices fall under?

Among its 41 most recently registered devices, the classes recorded for Marpac, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Marpac, Inc. in the registry?

The most recently registered devices listed for Marpac, Inc. include Marpac Inc 901-SSDD/107, Marpac Inc 203, Marpac Inc 951D and Marpac Inc 220SD.

Generated automatically from registry data and not verified by a human reviewer.