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Pro-Select Platinum®

FDA UDI

Class II (US FDA UDI)

by Den-Mat Holdings, LLC

Identity

Trade Name
Pro-Select Platinum® FDA UDI
Generic Name
Ultrasonic dental scaling/debridement system FDA UDI
Device Name
PSP SCALER HANDPIECE FDA UDI
Model / Reference
S40801 FDA UDI
Description
PSP SCALER HANDPIECE FDA UDI

Identifiers

Catalog Number
S40801 FDA UDI
Primary DI / UDI-DI
D813S408010 FDA UDI
510(k) Number
K964596 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Ultrasonic dental scaling/debridement system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ultrasonic dental scaling/debridement system

Pro-Select Platinum® by Den-Mat Holdings, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ultrasonic dental scaling/debridement system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 31851aa0-9c63-4477-9945-6aca02d1c147 37 fields · synced Jun 9, 2026