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Master-Dent

FDA UDI

by Dentonics, Inc.

Identity

Trade Name
MASTER-DENT FDA UDI
Generic Name
Orthodontic bracket adhesive FDA UDI
Device Name
Resin Cement, 7ml Dual Barrel Syringe w/ tips FDA UDI
Model / Reference
10-820 FDA UDI
Description
Resin Cement, 7ml Dual Barrel Syringe w/ tips FDA UDI

Identifiers

Primary DI / UDI-DI
00816526020176 FDA UDI
510(k) Number
K884081 FDA UDI
GMDN Term
Orthodontic bracket adhesive FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthodontic bracket adhesive

Master-Dent by Dentonics, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic bracket adhesive.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentonics, Inc.

Sources (1)

  • FDA UDI 989ea581-4b14-47e5-8d9e-a70b46f2b604 35 fields · synced May 30, 2026