GoldenDent

FDA UDI

Class I (US FDA UDI)

by GoldenDent

Identity

Trade Name: GoldenDent FDA UDI
Generic Name: Dental implant/prosthesis handling forceps FDA UDI
Device Name: Healing Abutment Forcep #1 75 Degree FDA UDI
Model / Reference: FS IA2 FDA UDI
Description: Healing Abutment Forcep #1 75 Degree FDA UDI

Identifiers

Catalog Number: FS IA2 FDA UDI
Primary DI / UDI-DI: 00850011211069 FDA UDI
FDA Product Code: LRW FDA UDI
GMDN Term: Dental implant/prosthesis handling forceps FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant/prosthesis handling forceps

GoldenDent by GoldenDent — 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: GoldenDent

Sources (1)

FDA UDI ec7a4af1-76d5-4e9e-8d27-2bae712f6091 34 fields · synced Jun 8, 2026