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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
Kit Contains: R227 Explorer 23/Probe UNC-12 R518 CSS-3 Gold Line™ Composite Sculpting System R362 113 Off Angle Cord Packer FDA UDI
Model / Reference
R909 - PDT Wallet 3 Pack - Doctor FDA UDI
Description
Kit Contains: R227 Explorer 23/Probe UNC-12 R518 CSS-3 Gold Line™ Composite Sculpting System R362 113 Off Angle Cord Packer FDA UDI

Identifiers

Catalog Number
R909 FDA UDI
Primary DI / UDI-DI
00813677025227 FDA UDI
FDA Product Code
DZN FDA UDI
EIY FDA UDI
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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental surgical probe, reusableDental spatula, reusableGingival retraction cord packing tool

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

Similar devices

Also classified as Gingival retraction cord packing tool.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PDT, Inc.

Sources (1)

  • FDA UDI e9b8c869-90f4-4fdf-8028-3c0aab9fe07d 34 fields · synced Jun 9, 2026