Identity

Trade Name
ORTHOCHEWIE FDA UDI
Generic Name
Orthodontic aligner/retainer seater, single-use FDA UDI
Device Name
ORTHOCHEWIE FOR ALIGNERS FDA UDI
Model / Reference
60.20.1003 FDA UDI
Description
ORTHOCHEWIE FOR ALIGNERS FDA UDI

Identifiers

Catalog Number
60.20.1003 FDA UDI
Primary DI / UDI-DI
07908611206053 FDA UDI
FDA Product Code
ECS FDA UDI
GMDN Term
Orthodontic aligner/retainer seater, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

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

Yes

FDA UDI

Category: Orthodontic aligner/retainer seater, single-use

Orthochewie by Orthometric - Industria E Comercio De Produtos Medicos E Odontologicos Ltda — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Orthodontic aligner/retainer seater, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f13835fb-1ec7-4247-8706-649152119b12 34 fields · synced May 29, 2026