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Resolve Ceramic

FDA UDI

Class I (US FDA UDI)

by Dentsply Sirona Orthodontics Inc.

Identity

Trade Name
Resolve Ceramic FDA UDI
Generic Name
Orthodontic bracket, ceramic FDA UDI
Device Name
Cer. ricketts .018 lower cuspid lhk each FDA UDI
Model / Reference
CRPL318LHK FDA UDI
Description
Cer. ricketts .018 lower cuspid lhk each FDA UDI

Identifiers

Catalog Number
CRPL318LHK FDA UDI
Primary DI / UDI-DI
D746CRPL318LHK1 FDA UDI
FDA Product Code
EJF FDA UDI
GMDN Term
Orthodontic bracket, ceramic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Resolve Ceramic by Dentsply Sirona Orthodontics Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bf214e9a-1341-42a1-9462-801537d51b9d 36 fields · synced Jun 9, 2026