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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, Screw, Six Web, Pink Strawberry FDA UDI
Model / Reference
103 (Screw) FDA UDI
Description
Prophy Cup, Screw, Six Web, Pink Strawberry FDA UDI

Identifiers

Catalog Number
103-P-1000 FDA UDI
Primary DI / UDI-DI
00813360020423 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 a6be2b28-c14f-48fc-b123-1d6467647f12 34 fields · synced Jun 6, 2026