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Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Dental polishing cup, reusable FDA UDI
Device Name
Prophy Angle Snap On FDA UDI
Model / Reference
1000261 FDA UDI
Description
Prophy Angle Snap On FDA UDI

Identifiers

Catalog Number
1000261 FDA UDI
Primary DI / UDI-DI
00304040057742 FDA UDI
510(k) Number
K073652 FDA UDI
FDA Product Code
EFB FDA UDI
GMDN Term
Dental polishing cup, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental polishing cup, reusable

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

Similar devices

Also classified as Dental polishing cup, reusable.

Cleared under the same submission

K073652 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Henry Schein, Inc.

Sources (1)

  • FDA UDI 8fd5c735-bdc1-44d9-9155-5eaca91926a0 35 fields · synced May 31, 2026