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Aqua Bond Composite

FDA UDI

Class II (US FDA UDI)

by Xemax Surgical Products, Inc.

Identity

Trade Name
Aqua Bond Composite FDA UDI
Generic Name
Orthodontic bracket adhesive FDA UDI
Device Name
Aqua Bond Compostie is a light cure, hydrophilic bracket adhesive, which can be applied to a dry or slightly contaminated surface. The smooth cohesive past viscosity allows for easy application to any style bracket base, insuring maximum mechanical retention. FDA UDI
Model / Reference
CLABC FDA UDI
Description
Aqua Bond Compostie is a light cure, hydrophilic bracket adhesive, which can be applied to a dry or slightly contaminated surface. The smooth cohesive past viscosity allows for easy application to any style bracket base, insuring maximum mechanical retention. FDA UDI

Identifiers

Catalog Number
CLABC FDA UDI
Primary DI / UDI-DI
D867CLABC0 FDA UDI
FDA Product Code
DYH FDA UDI
GMDN Term
Orthodontic bracket adhesive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3750 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Aqua Bond Composite by Xemax Surgical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Xemax Surgical Products, Inc.

Sources (1)

  • FDA UDI 7a07928f-0510-46f4-b67d-4c90ca0847c4 37 fields · synced May 30, 2026