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Retainer - Essex

FDA UDI

Class I (US FDA UDI)

by Digital Dental Laboratories, Inc

Identity

Trade Name
Retainer - Essex FDA UDI
Generic Name
Orthodontic retainer FDA UDI
Model / Reference
0043 FDA UDI

Identifiers

Primary DI / UDI-DI
00810126380043 FDA UDI
FDA Product Code
DYJ FDA UDI
GMDN Term
Orthodontic retainer 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic retainer

Retainer - Essex by Digital Dental Laboratories, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic retainer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 531282be-67ba-4401-9c96-9b624af5910c 32 fields · synced May 30, 2026