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Fli

FDA UDI

Class II (US FDA UDI)

by Rmo

Identity

Trade Name
FLI FDA UDI
Generic Name
Orthodontic bracket, ceramic FDA UDI
Device Name
FLI SIG ROTH MAX 1-2BIC .022R/L -7T W/HK FDA UDI
Model / Reference
Q07310 FDA UDI
Description
FLI SIG ROTH MAX 1-2BIC .022R/L -7T W/HK FDA UDI

Identifiers

Primary DI / UDI-DI
00885797116284 FDA UDI
FDA Product Code
NJM FDA UDI
GMDN Term
Orthodontic bracket, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 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

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: Orthodontic bracket, ceramic

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

Similar devices

Also classified as Orthodontic bracket, ceramic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rmo

Sources (1)

  • FDA UDI 9fd5a5c8-01fa-4941-8b95-be64ff2f2d39 33 fields · synced Jun 1, 2026