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Candid Aligner

FDA UDI

Class II (US FDA UDI)

by Candid Care Co.

Identity

Trade Name
Candid Aligner FDA UDI
Generic Name
Orthodontic progressive aligner FDA UDI
Device Name
Candid Aligner System FA-0001 FDA UDI
Model / Reference
FA-0001 FDA UDI
Description
Candid Aligner System FA-0001 FDA UDI

Identifiers

Primary DI / UDI-DI
00850004223567 FDA UDI
FDA Product Code
NXC FDA UDI
GMDN Term
Orthodontic progressive aligner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.5470 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthodontic progressive aligner

Candid Aligner by Candid Care Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic progressive aligner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Candid Care Co.

Sources (1)

  • FDA UDI a9aff8d1-e133-4cb4-bccc-f8cff0a06fb7 34 fields · synced Jun 1, 2026