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Silhouette

FDA UDI

Class I (US FDA UDI)

by Ortho Organizers, Inc.

Identity

Trade Name
Silhouette FDA UDI
Generic Name
Orthodontic bracket, ceramic FDA UDI
Device Name
Silhouette .022 LL4 HK -17T 0A 0O FDA UDI
Model / Reference
2886-374-5 FDA UDI
Description
Silhouette .022 LL4 HK -17T 0A 0O FDA UDI

Identifiers

Primary DI / UDI-DI
00190707007898 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Silhouette by Ortho Organizers, 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 8e7b0e40-6538-43d0-a29a-55b150c2c4a2 34 fields · synced Jun 9, 2026