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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
The Wingrove™ "Go-To" set includes: T005A-F A-Series FlipTop™ Cassette - Fixed Rack 5 R661 Wingrove™ B5-6 Ti R680 Wingrove™ L3-4 Ti R693 Wingrove™ N128 Blunt-Langer 5 Mini Ti T061 DiamondHead™ Ceramic Stone T216 EasyView™ UNC12 Probe FDA UDI
Model / Reference
R900 Wingrove™ Titanium Implant Instrument "Go-To" Set FDA UDI
Description
The Wingrove™ "Go-To" set includes: T005A-F A-Series FlipTop™ Cassette - Fixed Rack 5 R661 Wingrove™ B5-6 Ti R680 Wingrove™ L3-4 Ti R693 Wingrove™ N128 Blunt-Langer 5 Mini Ti T061 DiamondHead™ Ceramic Stone T216 EasyView™ UNC12 Probe FDA UDI

Identifiers

Catalog Number
R932 FDA UDI
Primary DI / UDI-DI
00813677024244 FDA UDI
FDA Product Code
EMN FDA UDI
EMS FDA UDI
FSM 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
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 00ee6f83-c507-4a19-b3f1-23dde543097b 34 fields · synced Jun 9, 2026