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Medicomp, Inc.

Also registered as Medicomp

United StatesFDA applicant, unverified FDA FEI 1033601

Medicomp, Inc. is a medical device manufacturer, with 93 devices listed in FDA GUDID and FDA 510(k) (FDA Class I and II) as of 13 Nov 2026.

Devices
93
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 70
  • FDA 510(k) 23

A device listed in two registries counts in both.

Device classes
  • FDA Class I 64
  • FDA Class II 29
Identifiers
  • FDA FEI 1033601
  • DUNS 057729253

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Medicomp, Inc. makes

Medicomp, Inc. manufactures single-use breathing circuit connectors, heat and moisture exchangers, and microbial medical gas filters. Their product portfolio also includes manual chest percussors, single-use anaesthesia breathing circuits, home-use electrocardiographs, medicine chamber spacers, and suction system plume particulate filters.

These products are listed in the FDA 510(k) and FDA UDI databases.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue93

Newest first, rows 1-50 of 93

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Company details

FDA FEI number
1033601
DUNS number
057729253
Address
600 Atlantis Rd, Melbourne, FL, 32904
Phone
8002343278

Frequently asked questions

How many devices does MEDICOMP, INC. have in the registry?

The registry currently lists 93 devices for MEDICOMP, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list MEDICOMP, INC.'s devices?

Among its 50 most recently registered devices, MEDICOMP, INC. has devices listed in FDA GUDID (50 devices).

What risk classes do MEDICOMP, INC.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for MEDICOMP, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from MEDICOMP, INC. in the registry?

The most recently registered devices listed for MEDICOMP, INC. include TelePatch Cardiac Monitor PM800, Hydrophobic Filter; 7mm M - 7mm M MC-250, HME without Gas Sampling Port; Angled MC-701NF and Single Straight Swivel Connector; 15F/22M - 15M MC-6490.

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