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E-Kit

FDA UDI

Class I (US FDA UDI)

by Tp Orthodontics, Inc.

Identity

Trade Name
E-Kit FDA UDI
Generic Name
Orthodontic inter-bracket elastic chain FDA UDI
Device Name
Grey FDA UDI
Model / Reference
384-000 FDA UDI
Description
Grey FDA UDI

Identifiers

Primary DI / UDI-DI
00192029037584 FDA UDI
FDA Product Code
ECI FDA UDI
GMDN Term
Orthodontic inter-bracket elastic chain 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic inter-bracket elastic chain

E-Kit by Tp Orthodontics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic inter-bracket elastic chain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0d27b7f5-bc12-4bac-bf50-ef0d0deaa9cf 33 fields · synced May 30, 2026