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Lotus Plus DS

FDA UDI

Class I (US FDA UDI)

by Ortho Technology, Inc.

Identity

Trade Name
Lotus Plus DS FDA UDI
Generic Name
Orthodontic bracket, metal FDA UDI
Device Name
Lotus Plus DS P D-STD 022 UR4/5 Rx -11° Tor. +2° Ang.+2OS(10PK) FDA UDI
Model / Reference
LPPD22-033 FDA UDI
Description
Lotus Plus DS P D-STD 022 UR4/5 Rx -11° Tor. +2° Ang.+2OS(10PK) FDA UDI

Identifiers

Primary DI / UDI-DI
00190730028730 FDA UDI
FDA Product Code
EJF FDA UDI
GMDN Term
Orthodontic bracket, metal 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

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

Yes

FDA UDI

Category: Orthodontic bracket, metal

Lotus Plus DS by Ortho Technology, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket, metal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 72b866b0-1a27-4a0e-aca9-9648a7864484 33 fields · synced May 30, 2026