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Avotec, Inc.

United Statesfrom the FDA registration address FDA FEI 1000113348

Avotec, Inc. is a medical device manufacturer, with 6 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.

Devices
6
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 5
  • FDA 510(k) 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 6
Identifiers
  • FDA FEI 1000113348
  • DUNS 802279984

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue6

Newest first, rows 1-6 of 6

Company details

FDA FEI number
1000113348
DUNS number
802279984
Address
609 N.W. BUCK HENDRY WAY, STUART, FL, 34994
Phone
7726920750

Frequently asked questions

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

The registry currently lists 6 devices for Avotec, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Avotec, Inc.'s devices?

Among its 6 most recently registered devices, Avotec, Inc. has devices listed in FDA 510(k) (1 device) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 6 most recently registered devices, the classes recorded for Avotec, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Avotec, Inc. include Silent Scan 3200, Silent Scan 3200/3300 Transducer, Silent Scan 3300 and SILENT SCAN.

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