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Paltop

FDA UDI

Class II (US FDA UDI)

by Paltop Advanced Dental Solutions, Ltd.

Identity

Trade Name
Paltop FDA UDI
Generic Name
Dental shaded pontic kit FDA UDI
Device Name
POP Kit Shade A3 FDA UDI
Model / Reference
45-70073 FDA UDI
Description
POP Kit Shade A3 FDA UDI

Identifiers

Catalog Number
45-70073 FDA UDI
Primary DI / UDI-DI
07290114693516 FDA UDI
FDA Product Code
ELM FDA UDI
GMDN Term
Dental shaded pontic kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3590 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

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
MRI Safety
MR Safe FDA UDI

Category: Dental shaded pontic kit

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

Similar devices

Also classified as Dental shaded pontic kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ae8d273d-3131-4abb-919a-a394b263bf11 35 fields · synced May 30, 2026