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Straumann Dental Implant System

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
STRAUMANN DENTAL IMPLANT SYSTEM FDA UDI
Generic Name
Dental prosthesis/implant abutment screw FDA UDI
Device Name
RC Basal Screw, TAN FDA UDI
Model / Reference
Screws FDA UDI
Description
RC Basal Screw, TAN FDA UDI

Identifiers

Catalog Number
025.4900 FDA UDI
Primary DI / UDI-DI
07630031712516 FDA UDI
510(k) Number
K062129 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental prosthesis/implant abutment screw FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3640 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental prosthesis/implant abutment screw

Straumann Dental Implant System by Institut Straumann SA — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental prosthesis/implant abutment screw.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e39a59df-aec3-4afa-b580-985bc4a66b0e 36 fields · synced Jun 8, 2026