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Button Bonder Tip

FDA UDI

Class I (US FDA UDI)

by Ortho Arch Company Inc

Identity

Trade Name
BUTTON BONDER TIP FDA UDI
Generic Name
Dental mould FDA UDI
Device Name
BUTTON BONDER TIP FDA UDI
Model / Reference
700-004T FDA UDI
Description
BUTTON BONDER TIP FDA UDI

Identifiers

Catalog Number
700-004T FDA UDI
Primary DI / UDI-DI
D909700004T1 FDA UDI
FDA Product Code
EGD FDA UDI
GMDN Term
Dental mould 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

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

No

FDA UDI

Category: Dental mould

Button Bonder Tip by Ortho Arch Company Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mould.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 48775532-dfdb-429f-9a18-cdcce30e3593 34 fields · synced Jun 8, 2026