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: R436 - The PDT Slade Blade™ 5 is designed for the Posterior Wide with smooth cutting edges on both ends. For the efficient removal of granulation tissue post extraction, 3.175mm blade. Designed with periodontist Dr. Scott Froum. The Slade Blade™ allows for more efficient removal of granulation tissue in post-extraction sockets because of a unique serrated edge and high-quality steel blade. Thorough removal of cystic infected tissue to leave a clean socket is crucial when preparing to place an implant. PDT’s Slade Blade™ line gives periodontists a more precise blade, sized more accurately for sockets. This allows for cleaner extractions and more effective implant placements. FDA UDI
Model / Reference: R436 Slade Blade 5, Posterior Wide Without Serrations FDA UDI
Description: R436 - The PDT Slade Blade™ 5 is designed for the Posterior Wide with smooth cutting edges on both ends. For the efficient removal of granulation tissue post extraction, 3.175mm blade. Designed with periodontist Dr. Scott Froum. The Slade Blade™ allows for more efficient removal of granulation tissue in post-extraction sockets because of a unique serrated edge and high-quality steel blade. Thorough removal of cystic infected tissue to leave a clean socket is crucial when preparing to place an implant. PDT’s Slade Blade™ line gives periodontists a more precise blade, sized more accurately for sockets. This allows for cleaner extractions and more effective implant placements. FDA UDI

Identifiers

Catalog Number: R436 FDA UDI
Primary DI / UDI-DI: 00813677022059 FDA UDI
FDA Product Code: EMK FDA UDI
GMDN Term: Periodontal curette 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Periodontal curette

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: PDT, Inc.

Sources (1)

FDA UDI da5b0092-2f55-4624-9d39-2c551439fcab 34 fields · synced Jun 9, 2026