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Paltop

FDA UDI

Class I (US FDA UDI)

by Paltop Advanced Dental Solutions, Ltd.

Identity

Trade Name
Paltop FDA UDI
Generic Name
Resilient dental precision attachment FDA UDI
Device Name
Paltop Equator Protective Disc Clear FDA UDI
Model / Reference
40-70288 FDA UDI
Description
Paltop Equator Protective Disc Clear FDA UDI

Identifiers

Catalog Number
40-70288 FDA UDI
Primary DI / UDI-DI
07290108699456 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Resilient dental precision attachment FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
Not 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

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

Yes

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
High-level Disinfectant FDA UDI

Paltop by Paltop Advanced Dental Solutions, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e1a9a16-d28a-4267-b7a8-96d88bc2f10c 36 fields · synced May 31, 2026