← Back to catalogue

Empower 2®

FDA UDI

Class I (US FDA UDI)

by American Orthodontics

Identity

Trade Name
Empower 2® FDA UDI
Generic Name
Orthodontic tube FDA UDI
Device Name
WELD TUBE SL EMPOWER UL 1ST MOLAR 018 SLOT T-18 A=0 R10D W/HK MES FDA UDI
Model / Reference
008-18-2618H FDA UDI
Description
WELD TUBE SL EMPOWER UL 1ST MOLAR 018 SLOT T-18 A=0 R10D W/HK MES FDA UDI

Identifiers

Catalog Number
008-18-2618H FDA UDI
Primary DI / UDI-DI
00190746132346 FDA UDI
FDA Product Code
DZD FDA UDI
GMDN Term
Orthodontic tube 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Empower 2® by American Orthodontics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 4eb24d04-052c-46f8-b987-8d8c2b7f4097 36 fields · synced Jun 9, 2026