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AllPro

FDA UDI

Class I (US FDA UDI)

by Team Technologies, Inc.

Identity

Trade Name
AllPro FDA UDI
Generic Name
Dental polishing cup, single-use FDA UDI
Device Name
Prophy Cup, Snap-On, Six Web, Aqua Vanilla FDA UDI
Model / Reference
303 (Snap On) FDA UDI
Description
Prophy Cup, Snap-On, Six Web, Aqua Vanilla FDA UDI

Identifiers

Catalog Number
303-A-144 FDA UDI
Primary DI / UDI-DI
00813360020638 FDA UDI
FDA Product Code
EHK FDA UDI
GMDN Term
Dental polishing cup, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6290 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

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: Dental polishing cup, single-use

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

Similar devices

Also classified as Dental polishing cup, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7ceccc5f-69f9-42f6-a376-7cc9ee70ce89 34 fields · synced Jun 6, 2026