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Titanium Healing Caps

FDA UDI

Class II (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
TITANIUM HEALING CAPS FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
RN healing cap, height 2.0 mm, titanium FDA UDI
Model / Reference
Healing / Closure Screws FDA UDI
Description
RN healing cap, height 2.0 mm, titanium FDA UDI

Identifiers

Catalog Number
048.033 FDA UDI
Primary DI / UDI-DI
07630031722294 FDA UDI
510(k) Number
K960634 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

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

Titanium Healing Caps 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.

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 81d22f0b-b07c-444d-8ba5-ccc9b97d870f 37 fields · synced May 30, 2026