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GP Implant System

FDA UDI

Class II (US FDA UDI)

by Gp - Implant Ltd

Identity

Trade Name
GP Implant System FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
Multiunit Screw FDA UDI
Model / Reference
GP-FSMU FDA UDI
Description
Multiunit Screw FDA UDI

Identifiers

Catalog Number
GP-FSMU FDA UDI
Primary DI / UDI-DI
07290018068625 FDA UDI
510(k) Number
K162299 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant system

GP Implant System by Gp - Implant Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gp - Implant Ltd

Sources (1)

  • FDA UDI 9e6ba5c1-2ca0-481b-b0bf-8507af7f3838 36 fields · synced May 30, 2026