← Back to catalogue

APC™ II Clarity™ SL

FDA UDI

Class II (US FDA UDI)

by 3m Unitek Corporation

Identity

Trade Name
APC™ II Clarity™ SL FDA UDI
Generic Name
Orthodontic bracket, ceramic FDA UDI
Device Name
Clarity(TM) SL Self-Ligating Bracket APC(TM) II High Torque VPO UL4,5 -4T/0A Hk .018 5/Pk FDA UDI
Model / Reference
3007-551 FDA UDI
Description
Clarity(TM) SL Self-Ligating Bracket APC(TM) II High Torque VPO UL4,5 -4T/0A Hk .018 5/Pk FDA UDI

Identifiers

Catalog Number
3007-551 FDA UDI
Primary DI / UDI-DI
00652221151414 FDA UDI
FDA Product Code
DYH FDA UDI
GMDN Term
Orthodontic bracket, ceramic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3750 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic bracket, ceramic

APC™ II Clarity™ SL by 3m Unitek Corporation — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 54a33e05-e296-4244-9661-36d92d7438af 35 fields · synced May 31, 2026