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MOR®-A Temporization Cap

FDA UDI

Class II (US FDA UDI)

by Sterngold Dental LLC

Identity

Trade Name
MOR®-A Temporization Cap FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Can be used to make a temporary crown. It can also be used as a base with which to create the final crown. FDA UDI
Model / Reference
904899 FDA UDI
Description
Can be used to make a temporary crown. It can also be used as a base with which to create the final crown. FDA UDI

Identifiers

Primary DI / UDI-DI
00841549113963 FDA UDI
510(k) Number
K171728 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
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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, permanent, preformed

MOR®-A Temporization Cap by Sterngold Dental LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

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 6ada43ba-9b25-45d2-94d6-7b076aebcc51 35 fields · synced May 30, 2026