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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 implantation drilling template retention pin FDA UDI
Device Name
Pin Fixation for Full Guided Surgery 25mm FDA UDI
Model / Reference
30-90003 FDA UDI
Description
Pin Fixation for Full Guided Surgery 25mm FDA UDI

Identifiers

Catalog Number
30-90003 FDA UDI
Primary DI / UDI-DI
07290108698886 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation drilling template retention pin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implantation drilling template retention pin

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 implantation drilling template retention pin.

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 47e6f017-f57e-4b92-acff-959ea5f9ee9a 35 fields · synced Jun 7, 2026