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: R226 - The PDT 23 Explorer-UNC15 Probe is a 23 Shepherd's Hook Explorer coupled with a UNC15 Probe with markings at 1-15mm. With two diagnostic instruments in one, this instrument is designed with efficiency in mind. FDA UDI
Model / Reference: R226 Explorer/Probe 23/UNC-15 FDA UDI
Description: R226 - The PDT 23 Explorer-UNC15 Probe is a 23 Shepherd's Hook Explorer coupled with a UNC15 Probe with markings at 1-15mm. With two diagnostic instruments in one, this instrument is designed with efficiency in mind. FDA UDI

Identifiers

Catalog Number: R226 FDA UDI
Primary DI / UDI-DI: 00813677021366 FDA UDI
FDA Product Code: EKB FDA UDI
EIX 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

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Single Use

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Implantable

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Contains Latex

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Prescription Use

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Over-the-Counter

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Convenience Kit

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Combination Product

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HCT/P

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Premarket Exempt

Yes

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Lot / Batch Number

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Serial Number

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Expiration Date

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Manufacturing Date

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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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: PDT, Inc.

Sources (1)

FDA UDI 2d68a7ec-e0ec-4767-aa0d-eda1812467a5 34 fields · synced Jun 9, 2026