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Dtc

FDA UDI

Class I (US FDA UDI)

by Hangzhou DTC Medical Apparatus Co., Ltd.

Identity

Trade Name
DTC FDA UDI
Generic Name
Self-ligating orthodontic bracket FDA UDI
Device Name
IN-Tendo JK-SL lingual brackets FDA UDI
Model / Reference
LSL74-17 FDA UDI
Description
IN-Tendo JK-SL lingual brackets FDA UDI

Identifiers

Primary DI / UDI-DI
06973554430019 FDA UDI
FDA Product Code
EJF FDA UDI
GMDN Term
Self-ligating orthodontic bracket FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.5410 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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
MRI Safety
MR Unsafe FDA UDI

Category: Self-ligating orthodontic bracket

Dtc by Hangzhou DTC Medical Apparatus Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Self-ligating orthodontic bracket.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7cdcf094-3e54-4367-92f5-b8e7c4c7c9fb 33 fields · synced May 30, 2026