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3D Dental

FDA UDI

Class I (US FDA UDI)

by 3d Dental Designs And Development, Llc

Identity

Trade Name
3D Dental FDA UDI
Generic Name
Orthodontic appliance relief material FDA UDI
Device Name
Patient Size Orthodontic Wax 50/Bx FDA UDI
Model / Reference
30801 FDA UDI
Description
Patient Size Orthodontic Wax 50/Bx FDA UDI

Identifiers

Catalog Number
30801 FDA UDI
Primary DI / UDI-DI
00817169029656 FDA UDI
FDA Product Code
EGD FDA UDI
GMDN Term
Orthodontic appliance relief material FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6890 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

Yes

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

No

FDA UDI

Category: Orthodontic appliance relief material

3D Dental by 3d Dental Designs And Development, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic appliance relief material.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9813b48d-977a-476c-87b8-984e4d358205 34 fields · synced May 30, 2026