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PDT, Inc.

Active in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000045324 FEI 3003963832

PDT, Inc. is a medical device manufacturer based in the United States, with 536 devices listed in FDA GUDID and EUDAMED (FDA Class I and II; EU Class I) as of 15 Nov 2026.

Devices
536
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 15 Nov 2026

Registries
  • FDA GUDID 536
  • EUDAMED 177

A device listed in two registries counts in both.

Device classes
  • FDA Class I 531
  • FDA Class II 3
  • EU Class I 2
Top EMDN categories
Identifiers
  • EUDAMED SRN US-MF-000045324
  • FDA FEI 3003963832
  • DUNS 125850144

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA FEI

What PDT, Inc. makes

PDT, Inc. manufactures reusable manual dental instruments including periodontal curettes, manual dental scalers, dental surgical probes, instrument trays, surgical soft-tissue manipulation forceps, manual non-rotary dental instrument handles, dental restoration carvers, and dental mirrors.

The company's devices are classified as Class I and Class II and are listed in both eudamed and fda_udi registries. PDT, Inc. is based in the US.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue536

Newest first, rows 1-50 of 536

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Rows 1-50 of 536

Showing 1-50 of 536

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000045324
SRN (system / procedure pack)
US-PR-000045246
FDA FEI number
3003963832
DUNS number
125850144
EUDAMED status
Active
EUDAMED registered name
PDT, Inc.
EUDAMED abbreviated name
PDT
Registered address
8275 US Highway 10 W, 59808, Missoula, United States
Website
pdtdental.com
Phone
1-406-626-4153
PRRC contact
Tanya Ochoa(public in EUDAMED)

Frequently asked questions

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

The registry currently lists 536 devices for PDT, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list PDT, Inc.'s devices?

Among its 50 most recently registered devices, PDT, Inc. has devices listed in EUDAMED (16 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.

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

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

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

The most recently registered devices listed for PDT, Inc. include PDT, Inc., PDT, Inc. H5-N128, Montana Black 23 and Boge Precision Duo.

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