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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
Dental soft-tissue coring punch, single-use FDA UDI
Device Name
Tissue Punch Ø5mm FDA UDI
Model / Reference
60-70141 FDA UDI
Description
Tissue Punch Ø5mm FDA UDI

Identifiers

Catalog Number
60-70141 FDA UDI
Primary DI / UDI-DI
07290108698879 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Dental soft-tissue coring punch, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental soft-tissue coring punch, single-use

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

Similar devices

Also classified as Dental soft-tissue coring punch, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Paltop Advanced Dental Solutions, Ltd.

Sources (1)

  • FDA UDI 31c14434-8cca-4d17-bd25-b5f0ea8fe101 35 fields · synced Jun 1, 2026