RP Low Margin Abutment 2.0mm Cuff

FDA UDI

Class II (US FDA UDI)

by Sterngold Dental LLC

Identity

Trade Name: RP Low Margin Abutment 2.0mm Cuff FDA UDI
Generic Name: Dental implant suprastructure, permanent, preformed FDA UDI
Device Name: The RP Low Margin Abutments allow for more aesthetic restorations than are possible with conventional standard abutments. Due to the abutment's conical shape, restorative components are unique to the system; yet the same restorative procedures and instrumentation are used. Available in 1.0mm, 2.0mm, 3.0mm, 4.0mm, 5.0mm cuff sizes. They accommodate up to 25% of total divergence between implants. Small diameter allows use at mandibular anterior sites. Intended for use with dental implants to support and/or retain removable dental prostheses in the treatment of partially or totally edentulous patients to restore chewing function. The abutment screws directly into endosseous implants or they screw into Abutment Bases which are screwed into endosseous implants. FDA UDI
Model / Reference: 904353 FDA UDI
Description: The RP Low Margin Abutments allow for more aesthetic restorations than are possible with conventional standard abutments. Due to the abutment's conical shape, restorative components are unique to the system; yet the same restorative procedures and instrumentation are used. Available in 1.0mm, 2.0mm, 3.0mm, 4.0mm, 5.0mm cuff sizes. They accommodate up to 25% of total divergence between implants. Small diameter allows use at mandibular anterior sites. Intended for use with dental implants to support and/or retain removable dental prostheses in the treatment of partially or totally edentulous patients to restore chewing function. The abutment screws directly into endosseous implants or they screw into Abutment Bases which are screwed into endosseous implants. FDA UDI

Identifiers

Primary DI / UDI-DI: 00841549111150 FDA UDI
510(k) Number: K946198 FDA UDI
FDA Product Code: NHA FDA UDI
GMDN Term: Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 872.3630 FDA UDI
Commercial Distribution: Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

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

RP Low Margin Abutment 2.0mm Cuff by Sterngold Dental LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 II	Pending data

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Manufacturer

Manufacturer: Sterngold Dental LLC

Sources (1)

FDA UDI cbc1d9e7-dbba-45c4-b2ab-938dc2fff3f8 36 fields · synced May 30, 2026