Paltop

FDA UDI

Class I (US FDA UDI)

by Paltop Advanced Dental Solutions, Ltd.

Identity

Trade Name: Paltop FDA UDI
Generic Name: Fixture/appliance dental drill bit, reusable FDA UDI
Device Name: Fully Guided Drill Ø5mm L30mm FDA UDI
Model / Reference: 30-70322 FDA UDI
Description: Fully Guided Drill Ø5mm L30mm FDA UDI

Identifiers

Catalog Number: 30-70322 FDA UDI
Primary DI / UDI-DI: 07290108697964 FDA UDI
FDA Product Code: DZA FDA UDI
GMDN Term: Fixture/appliance dental drill bit, reusable 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Fixture/appliance dental drill bit, reusable

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Paltop Advanced Dental Solutions, Ltd.

Sources (1)

FDA UDI 59dd1ed0-d2a8-48c5-98de-2bb76e3c3705 35 fields · synced Jun 8, 2026