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Rmo

FDA UDI

Class II (US FDA UDI)

by Rmo

Identity

Trade Name
RMO FDA UDI
Generic Name
Subperiosteal dental implant material FDA UDI
Device Name
BUTTON MINI IMPLANT DIA1.4L6MM FDA UDI
Model / Reference
G00111 FDA UDI
Description
BUTTON MINI IMPLANT DIA1.4L6MM FDA UDI

Identifiers

Primary DI / UDI-DI
00885797096159 FDA UDI
FDA Product Code
DZE FDA UDI
GMDN Term
Subperiosteal dental implant material 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Subperiosteal dental implant material

Rmo by Rmo — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Subperiosteal dental implant material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rmo

Sources (1)

  • FDA UDI 2f78af3b-30aa-4153-8368-ca57c39465b9 33 fields · synced May 31, 2026