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PDT, Inc.

FDA UDI

Class I (US FDA UDI)

by PDT, Inc.

Identity

Trade Name
PDT, Inc. FDA UDI
Generic Name
Dental surgical probe, reusable FDA UDI
Device Name
R170 - The PDT Montana Explorer™ is the perfect companion for the Montana Jack, featuring the same contra-angle providing better universal adaptation. FDA UDI
Model / Reference
R170 Montana Explorer FDA UDI
Description
R170 - The PDT Montana Explorer™ is the perfect companion for the Montana Jack, featuring the same contra-angle providing better universal adaptation. FDA UDI

Identifiers

Catalog Number
R170 FDA UDI
Primary DI / UDI-DI
00813677021151 FDA UDI
FDA Product Code
EKB FDA UDI
GMDN Term
Dental surgical probe, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental surgical probe, reusable

PDT, Inc. by PDT, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental surgical probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PDT, Inc.

Sources (1)

  • FDA UDI 2f8da7ee-61ef-4247-8d3c-190b3f5fe173 35 fields · synced Jun 9, 2026