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MOR® RC-2 10 pack

FDA UDI

Class II (US FDA UDI)

by Sterngold Dental LLC

Identity

Trade Name
MOR® RC-2 10 pack FDA UDI
Generic Name
Resilient dental precision attachment FDA UDI
Device Name
A female part which is inserted into the acrylic overdenture and houses changeable nylon retention inserts. FDA UDI
Model / Reference
904815 FDA UDI
Description
A female part which is inserted into the acrylic overdenture and houses changeable nylon retention inserts. FDA UDI

Identifiers

Primary DI / UDI-DI
00841549115721 FDA UDI
510(k) Number
K153173 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Resilient dental precision attachment 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

No

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: Resilient dental precision attachment

MOR® RC-2 10 pack by Sterngold Dental LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Resilient dental precision attachment.

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 640a32c9-4f89-4683-b464-ebe68241ad34 35 fields · synced Jun 8, 2026