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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 elevator, tooth/root FDA UDI
Device Name
T102S Root elevator Seldin No. 301 straight Smooth Handle FDA UDI
Model / Reference
T102S Root elevator Seldin No. 301 straight Smooth Handle FDA UDI
Description
T102S Root elevator Seldin No. 301 straight Smooth Handle FDA UDI

Identifiers

Catalog Number
T102S FDA UDI
Primary DI / UDI-DI
00813677024190 FDA UDI
FDA Product Code
EMJ FDA UDI
GMDN Term
Dental elevator, tooth/root 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 elevator, tooth/root

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

Similar devices

Also classified as Dental elevator, tooth/root.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PDT, Inc.

Sources (1)

  • FDA UDI d76e4a21-ca69-43bf-b52d-9aceda818882 34 fields · synced Jun 9, 2026