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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
Periodontal curette FDA UDI
Device Name
Kit Includes: T005A-F FlipTop™ Cassette 'A' - Fixed Rack 5 R096 N1 R139 N2 R138BC Montana Jack® (Breast Cancer Pink) R064 Columbia 13-14 R130S Jack B. Nimble® Slim Scaler FDA UDI
Model / Reference
R977 Gingival Inflammation Kit FDA UDI
Description
Kit Includes: T005A-F FlipTop™ Cassette 'A' - Fixed Rack 5 R096 N1 R139 N2 R138BC Montana Jack® (Breast Cancer Pink) R064 Columbia 13-14 R130S Jack B. Nimble® Slim Scaler FDA UDI

Identifiers

Catalog Number
R977 FDA UDI
Primary DI / UDI-DI
00813677024527 FDA UDI
FDA Product Code
EMS FDA UDI
EMN FDA UDI
FSM FDA UDI
GMDN Term
Periodontal curette 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, reusable

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

Similar devices

Also classified as Manual dental scaler, 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 25610616-a2cc-4279-8baa-d621ba25600f 34 fields · synced Jun 9, 2026