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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
Manual dental scaler, reusable FDA UDI
Device Name
Kit Containing: R138T - Montana Jack Titanium R696 - Amazing Gracey 13-14 Titanium Extended Reach Micro Mini R630 - Pineyro Arch Ti1 R631 - Pineyro Arch Ti2 R632 - Pineyro Arch Ti3 R633 - Pineyro Arch Ti4 R661 - Wingrove B 5-6 Titanium Implant R680 - Wingrove L 3-4 Titanium Implant R693 - Wingrove N128 Blunt-Langer 5 Mini Titanium Implant T216 - EasyView UNC12 Probe T061 - Diamond Head Ceramic Stone E-Z Jett Cassette 10-Place FDA UDI
Model / Reference
R932 Ultimate Implant Kit FDA UDI
Description
Kit Containing: R138T - Montana Jack Titanium R696 - Amazing Gracey 13-14 Titanium Extended Reach Micro Mini R630 - Pineyro Arch Ti1 R631 - Pineyro Arch Ti2 R632 - Pineyro Arch Ti3 R633 - Pineyro Arch Ti4 R661 - Wingrove B 5-6 Titanium Implant R680 - Wingrove L 3-4 Titanium Implant R693 - Wingrove N128 Blunt-Langer 5 Mini Titanium Implant T216 - EasyView UNC12 Probe T061 - Diamond Head Ceramic Stone E-Z Jett Cassette 10-Place FDA UDI

Identifiers

Catalog Number
R932 FDA UDI
Primary DI / UDI-DI
00813677029324 FDA UDI
FDA Product Code
EMN FDA UDI
EMS FDA UDI
EIX FDA UDI
FSM FDA UDI
GMDN Term
Manual dental scaler, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
878.4800 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

Yes

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: Instrument tray, reusablePeriodontal curetteManual dental scaler, reusableDental 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 913e534a-06e3-48b4-ae19-5a39dbced7c0 34 fields · synced Jun 9, 2026