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All-Bond 2

FDA UDI

Class II (US FDA UDI)

by Bisco Inc.

Identity

Trade Name
All-Bond 2 FDA UDI
Generic Name
Dentine bonding agent/set FDA UDI
Device Name
Pre-Bond Resin 6ml Bottle Pkg FDA UDI
Model / Reference
B-2506A FDA UDI
Description
Pre-Bond Resin 6ml Bottle Pkg FDA UDI

Identifiers

Catalog Number
B-2506A FDA UDI
Primary DI / UDI-DI
00810111542005 FDA UDI
510(k) Number
K910860 FDA UDI
FDA Product Code
KLE FDA UDI
GMDN Term
Dentine bonding agent/set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3200 FDA UDI
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

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

Yes

FDA UDI

Category: Dentine bonding agent/set

All-Bond 2 by Bisco Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dentine bonding agent/set.

Cleared under the same submission

K910860 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bisco Inc.

Sources (1)

  • FDA UDI 01bafe2a-3408-4177-b014-9e98dc633109 37 fields · synced Jun 1, 2026