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Prescott'S, Inc.

United StatesFDA applicant, unverified FDA FEI 1721685

Prescott'S, Inc. is a medical device manufacturer, with 4 devices listed in FDA 510(k) and FDA GUDID (FDA Class I and II) as of 12 Nov 2026.

Devices
4
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 12 Nov 2026

Registries
  • FDA 510(k) 2
  • FDA GUDID 2

A device listed in two registries counts in both.

Device classes
  • FDA Class I 3
  • FDA Class II 1
Identifiers
  • FDA FEI 1721685
  • DUNS 151053444

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue4

Newest first, rows 1-4 of 4

Company details

FDA FEI number
1721685
DUNS number
151053444
Address
18940 Microscope Way, Monument, CO, 80132

Frequently asked questions

How many devices does Prescott'S, Inc. have in the registry?

The registry currently lists 4 devices for Prescott'S, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Prescott'S, Inc.'s devices?

Among its 4 most recently registered devices, Prescott'S, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 4 most recently registered devices, the classes recorded for Prescott'S, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Prescott'S, Inc. in the registry?

The most recently registered devices listed for Prescott'S, Inc. include OSM200 Stand PMPLP-KS000, Prescott’s Wall Mount Surgical Microscope Platform PMPLP-WM000 - WALL MOUNT, PRESCOTT'S SURGICAL SPEAR and MICROSCOPE KNOB COVER, STERILE, DISPOSABLE.

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