OptiBond Solo Plus

Single-Component, Total-Etch Bonding Agent; 100-Pack Unidose Packets

Registry build 21.09.26
6manufacturers in China registered for this device type
5catalogue numbers in this listing
4510(k) clearances naming this product code
11recalls on this code

Who Else Makes It

Concentrated in Jilin (2), Liaoning (1), Guangdong (1).

Chinese manufacturers registered for FDA product code KLE
Manufacturer City Province Registered as Device types
Liaoning Upcera Co., Ltd. Benxi Liaoning Contract manufacturer 10
Shenzhen Upcera Digital Dental Technology Co., Ltd. Shenzhen Guangdong Exporter 10
Rizhao Huge Biomaterials Company, Ltd. Rizhao Shandong Manufacturer 7
CAO (China) Medical Equipment Company, Limited Langfang Hebei Contract manufacturer 6
Sincera Technology (Changchun) Co., Ltd. Changchun Jilin Manufacturer 2
Sino-Dentex Co., Ltd. Changchun Jilin Manufacturer 2

Record

Regulatory record for OptiBond Solo Plus
Listed by Kerr Corporation, United States
FDA product code KLE
Device type Agent, Tooth Bonding, Resin
Device class Class 2
Regulation 21 CFR 872.3200
Establishment Contract manufacturer, Reprocessor, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2016-08-01
Record revised 2025-05-06 (version 5)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Storage Storage environment temperature 2 to 25 °C
Packaging Bag, box of 100
Sizes Total volume 0.2 to 10 ml

Catalogue Numbers

Catalogue numbers for OptiBond Solo Plus
Catalogue number Size Per pack Status
29669 Total Volume 10 ml 100 In distribution
29682 Total Volume 10 ml In distribution
31513 Total Volume 5 ml In distribution
33677 Total Volume.2 ml 2 In distribution
31514 Total Volume 10 ml In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Epic® Parkell, Inc. 22
All-Bond Universal Bisco, Inc. 18
Henry Schein Henry Schein, Inc. 16
Peak Universal Bond Ultradent Products Inc. 16
Brush&Bond® Parkell, Inc. 16
All-Bond 2 Bisco, Inc. 15
The Orthodontic Store Young Innovations Inc. 15
All-Bond 3 Bisco, Inc. 13
Scotchbond™ Universal 3M Deutschland GmbH 13
Select HV Etch w/BAC Bisco, Inc. 12
Prelude Danville Materials, LLC 12
Jade Dharma Research, Inc. 12

Showing 12 of 609. All products under Agent, Tooth Bonding, Resin

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K222830 2023-01-12
K182162 2018-11-07
K101423 2010-07-30
K100347 2010-04-30

Recalls

The FDA has not published a severity grade for these. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2010-05-27 Not classified Nonconforming Material/Component The recall was initiated because Pentron Clinical has confirmed that various lots of Bond-1 Primer/Adhesive have been found to have gelled and therefore becomes unusable. 30,276 units total 2012-03-02
2009-08-24 Not classified Nonconforming Material/Component Some of the material has been found to be gelled and therefore becomes unusable. 1,400 2012-02-24
2006-08-29 Not classified Other Mis-pack/mis-label: The OptiBond Self Etch Primer and OptiBond Solo Plus Adhesive in the chambers were mis-packaged/mis-labeled in reverse order. Application of these products in reverse order may result in compromised bond strength. 247 Kits (50 unidose pouches/Kit) 2012-08-03
2006-03-03 Not classified Other The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance. 85 2012-03-07
2006-03-03 Not classified Other The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance. 34 2012-03-07
2006-03-03 Not classified Other The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance. 6898 2012-03-07
2006-03-03 Not classified Other The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance. 161 2012-03-07
2006-03-03 Not classified Other The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance. 40 2012-03-07
2006-03-03 Not classified Other The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance. 16 2012-03-07
2006-03-03 Not classified Other The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance. 72 2012-03-07
2006-03-03 Not classified Other The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance. 10 2012-03-07

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer