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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 implant abutment analog, intraoral-scanning, single-use FDA UDI
Device Name
Digital Analog SP FDA UDI
Model / Reference
30-70501 FDA UDI
Description
Digital Analog SP FDA UDI

Identifiers

Catalog Number
30-70501 FDA UDI
Primary DI / UDI-DI
07290108695014 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant abutment analog, intraoral-scanning, single-use 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

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

Category: Dental implant abutment analog, intraoral-scanning, 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 implant abutment analog, intraoral-scanning, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI add1ed75-d5f0-40ba-9db0-7dff5d649d6a 35 fields · synced Jun 1, 2026