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KERR CORPORATION

Last updated September 17, 2026

What KERR CORPORATION makes

The company produces dental restorative materials, including light-cured and conventional composite resin fillings, preformed root canal posts, and dentine bonding agents. It also manufactures silicone impression materials for dental molds, porcelain/ceramic restoration kits, and single-use rotary/reciprocating endodontic files. Additional products include sterilization packaging and dispensing tools for dental applications.

These devices are regulated under FDA classifications, including Class I, Class II, and Unclassified (U), and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Kerr Corporation manufacture?

Kerr Corporation specializes in dental devices, primarily producing restorative materials like light-cured and conventional composite resin fillings (e.g., Herculite XRV, Flow-It ALC). It also manufactures preformed root canal posts (e.g., Point 4), dentine bonding agents (e.g., Take 1 Advanced), silicone dental impression materials, porcelain/ceramic restoration kits, and single-use rotary/reciprocating endodontic files (e.g., FibreKleer 4x). Additional products include sterilization packaging and dental dispensing tools, all designed for dental procedures.

Where is Kerr Corporation based, and how does that affect its devices?

Kerr Corporation is based in the United States, which means its devices are subject to FDA regulations. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. medical device standards. The U.S. regulatory framework applies to classifications like Class I (low-risk devices), Class II (moderate-risk devices requiring special controls), and Unclassified (U) devices, depending on the specific product.

Which regulatory registries list Kerr Corporation’s devices?

Kerr Corporation’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system assigns a unique product code to each device, enabling tracking, transparency, and compliance verification. This registry is essential for healthcare providers, regulators, and supply chain partners to identify and validate the devices in use.

How are Kerr Corporation’s devices classified under FDA regulations?

Kerr Corporation’s devices fall into different FDA classifications based on risk and intended use. Light-cured composites and bonding agents, for example, are often classified as Class II due to their moderate risk and need for performance standards. Single-use items like rotary files or sterilization packaging may qualify as Class I (lower risk) or Unclassified (U) if they don’t fit standard Class I/II criteria. Classification determines regulatory requirements, such as pre-market submissions or post-market surveillance.

What kinds of dental materials does Kerr Corporation focus on, and why are these important?

Kerr Corporation focuses on dental restorative and impression materials, including composite resins (for fillings), silicone impression materials (for molds), and porcelain/ceramic kits (for durable restorations). These materials are critical in dental procedures because they restore function and aesthetics, seal teeth to prevent decay, and create accurate molds for crowns or bridges. The company’s products are designed to meet clinical needs while adhering to regulatory standards for safety and efficacy.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: 1889 W Mission Blvd, Pomona, CA, 91766
Website: kavokerrgroup.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +18005377123
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3012477813
DUNS Number: 847905890

Catalogue (1488)

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Device	Model / Reference	Registries	Class	Status
Harmonize	36441	FDA UDI	Class II	Active
SoftLine	32238	FDA UDI	Class II	Active
High Spot	27080	FDA UDI	Class I	Active
Impression Tray	Q17C	FDA UDI	Class I	Active
Gingival / Opaque	34678	FDA UDI	Class II	Active
Correct Plus	Q34HCA	FDA UDI	Class II	Active
OptiBond All-In-One	33535	FDA UDI	Class II	Active
Expasyl	31172	FDA UDI	U	Active
Correct Plus	Q36B	FDA UDI	Class II	Active
Simile	N56BS	FDA UDI	Class II	Active
Premise	32652	FDA UDI	Class II	Active
Point 4	29916	FDA UDI	Class II	Active
Build-It FR	N32AC	FDA UDI	Class II	Active
Kolor + Plus	23403	FDA UDI	Class II	Active
Crown Test Tip	973-0309	FDA UDI	Class II	Active
Disposable Intraoral Syringe Tips	20731	FDA UDI	Class I	Active
Herculite Ultra	35488	FDA UDI	Class II	Active
SonicFill 3	36711	FDA UDI	Class II	Active
Correct Plus	Q36MA	FDA UDI	Class II	Active
BioPlant	216112	FDA UDI	Class II	Active
PeelVue Pro	37068	FDA UDI	Class II	Active
Ultrasonic Tips	973-0057	FDA UDI	Class II	Active
Alert	N15SB	FDA UDI	Class II	Active
Take 1 Advanced	33959	FDA UDI	Class II	Active
Point 4	29918	FDA UDI	Class II	Active
FibreKleer 4x	N81CC	FDA UDI	Class I	Active
Premise Indirect	33606	FDA UDI	Class II	Active
Flow-It ALC	N11J	FDA UDI	Class II	Active
FibreKor	N18AD	FDA UDI	Class I	Active
Herculite Ultra	35626	FDA UDI	Class II	Active
Take 1 Advanced	33968	FDA UDI	Class II	Active
Opaque	800-126	FDA UDI	Class II	Active
Permlastic	00677	FDA UDI	Class II	Active
Point 4	29881	FDA UDI	Class II	Active
Flow-It ALC	N11VXB	FDA UDI	Class II	Active
Cement-It Universal C&B	N33AC	FDA UDI	Class II	Active
Herculite Ultra	34353	FDA UDI	Class II	Active
Herculite XRV	29836	FDA UDI	Class II	Active
Herculite XRV	29824	FDA UDI	Class II	Active
OptiDisc	33484	FDA UDI	Class I	Active
Nexus Universal Automix Tips - Wide 50pk	37000	FDA UDI	Class II	Active
Point 4	31369	FDA UDI	Class II	Active
Herculite Ultra	35491	FDA UDI	Class II	Active
Kolor + Plus	23402	FDA UDI	Class II	Active
Flex Tab	004-008	FDA UDI	Class I	Active
Premise	32658	FDA UDI	Class II	Active
Point 4	29685	FDA UDI	Class II	Active
Herculite XRV	29837	FDA UDI	Class II	Active
Artiste	N36AK	FDA UDI	Class II	Active
CoreRestore2	31748	FDA UDI	Class II	Active

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FDA Recalls (64)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Kerr Corporation has initiated 64 recall records between March 3, 2006, and May 29, 2014, all of which are recorded as terminated. The recalls involve dental and medical devices, with reasons including permanent marking issues (e.g., laser loupes), material defects (e.g., resin separation, stiffening, or improper curing), mis-packaging/mis-labeling (e.g., adhesive products reversed), performance inconsistencies (e.g., bonding failure, flowability issues), and component malfunctions (e.g., polymerized catalyst, incorrect electronics in headlights). Some recalls cite deviations from specified behavior, such as faster-than-expected setting times or altered handling properties.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
May 29, 2014	Z-1788-2014	—	terminated	Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number 29948, Lot Number 3-1294), because it may set faster than specified in the Directions for Use.
Oct 25, 2012	Z-0401-2013	—	terminated	The firm initiated the recall becaue disturbing the BioPlant product soon after it is placed may halt or delay the ossification process.
Apr 10, 2012	Z-0414-2013	—	terminated	The firm initiated the recall for Laser Loupes because the ink used to mark which laser frequency each laser Loupe protects against may wipe off. The loupes work according to specification, but the marking may not permanently adhere to the device.
Feb 21, 2012	Z-0268-2013	—	terminated	The firm recalled the product because it may cure harder than expected within the shelf life, which could result in a material that may be more difficult to remove. Use of this product on patients with loose teeth may result in possible tooth fracture or tooth extraction.
Nov 17, 2011	Z-0402-2013	—	terminated	The firm recalled the Freedom Cordless LED Headlight because some units were assembled with an incorrect component in the control board electronics that may cause some Freedom Cordless LED Headlight units to become warm to the touch; however, no skin damage will occur.
Mar 3, 2011	Z-1205-2012	—	terminated	The recall was initiated because Pentron Clinical has confirmed that the TempSpan Temporary Cement may have black plastic material on the surface of the paste, and it may set faster than specified.
Mar 3, 2011	Z-0455-2012	—	terminated	The resin material separates when the product is extruded from the syringe. Although there are no safety issues related with this situation, please refrain from using the affected product.
Feb 3, 2011	Z-0915-2012	—	terminated	The recall was initiated because Kerr Corporation has confirmed that the use of the affected lot of Maxcem Elite may not provide users with a minimum of 2 minutes of worktime thereby causing the product to prematurely set by 15 seconds.
Dec 2, 2010	Z-1100-2012	—	terminated	The recall was initiated because Pentron Clinical has confirmed that the Breeze Self-Adhesive Resin Cement exhibits faster than expected gel and set times. If the work time is exceeded when using this material, it could possibly result in inadequate bond strength.
Aug 19, 2010	Z-1115-2012	—	terminated	A recall was initiated because Pentron Clinical has confirmed that the Fusio Liquid Dentin is not as flowable as ideally expected.
May 27, 2010	Z-1142-2012	—	terminated	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.
Sep 9, 2009	Z-0074-2010	—	terminated	The recall was initiated because the catalyst portion of the syringe may have polymerized, therefore making the product unusable.
Sep 5, 2008	Z-0241-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0255-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0270-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0251-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0244-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0230-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0267-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0240-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0235-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0259-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0258-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0254-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0252-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0232-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0243-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0269-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0260-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0268-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0264-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0250-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0239-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0234-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0242-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0247-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0257-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0231-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0238-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0249-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0233-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0261-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0256-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0237-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0246-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0265-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0236-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0245-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0253-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0248-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0229-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0266-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0262-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Sep 5, 2008	Z-0263-2009	—	terminated	Material stiff: Material in several lots of Premise Unidose appears to stiffen and become difficult to extrude over time.
Aug 29, 2006	Z-1521-06	—	terminated	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.
Aug 14, 2006	Z-1524-06	—	terminated	Low Bonding performance: The affected lots of product may not activate properly, which may cause lower than expected bonding performance (due to a low level of chemical cure initiator in the lots manufactured)
Mar 3, 2006	Z-0689-06	—	terminated	The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance.
Mar 3, 2006	Z-0693-06	—	terminated	The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance.
Mar 3, 2006	Z-0691-06	—	terminated	The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance.
Mar 3, 2006	Z-0690-06	—	terminated	The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance.
Mar 3, 2006	Z-0686-06	—	terminated	The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance.
Mar 3, 2006	Z-0692-06	—	terminated	The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance.
Mar 3, 2006	Z-0688-06	—	terminated	The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance.
Mar 3, 2006	Z-0687-06	—	terminated	The affected lot of product may not activate properly throughout the full intended shelf life and may result in lower than expected bonding performance.