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Straumann Extraoral Implant System

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
STRAUMANN EXTRAORAL IMPLANT SYSTEM FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
EO Healing cap, D 3.5mm, L 3.8mm, Ti FDA UDI
Model / Reference
EO FDA UDI
Description
EO Healing cap, D 3.5mm, L 3.8mm, Ti FDA UDI

Identifiers

Catalog Number
048.044 FDA UDI
Primary DI / UDI-DI
07630031722409 FDA UDI
510(k) Number
K990458 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use 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

Dimensions & Sizes

Size
Length — 3.8 Millimeter FDA UDI
Outer Diameter — 3.5 Millimeter FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

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

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4163d991-c642-4f24-b9dd-700f05d01600 37 fields · synced May 30, 2026