Data / Medical devices / United States / Kerr Corporation

Kerr Corporation: FDA-registered device maker in Pomona, CA, United States, 4 510(k) clearances

Name: Kerr Corporation FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Kerr Corporation is registered with the FDA (registration 3032378317) in Pomona, CA, United States. It lists 11 device types. The FDA files 4 510(k) clearances under its listings, the newest dated August 17, 2015. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3032378317
Address: 1937 W Mission Blvd, Pomona, CA, United States, 91766
Owner or operator: SYBRON DENTAL SPECIALTIES, INC. (9029565)
Roles: Complaint file establishment, Contract manufacturer, Manufacturer, Specification developer
First device listed: December 15, 1982
Registered through: 2026
Brand names listed: Adapt Luciwedge, All Ceramic Logic Set, All-Purpose Esthetic Logic Set, Artiste Nano Composite, Axis Carbide Burs, Barbed Broaches, Biosplint Adhesive, BluWhite Carbides and more

Devices it lists

Device	Product code	Class	Role	Source
Adhesive, Bracket And Tooth Conditioner, Resin	DYH	2	Contract manufacturer	accessdata.fda.gov
Agent, Tooth Bonding, Resin	KLE	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Bur, Dental	EJL	1	Manufacturer	accessdata.fda.gov
Cement, Dental	EMA	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Cleanser, Root Canal	KJJ	U	Contract manufacturer	accessdata.fda.gov
Crown And Bridge, Temporary, Resin	EBG	2	Contract manufacturer	accessdata.fda.gov
Dental Cement W/Out Zinc-Oxide Eugenol As An Ulcer Covering For Pain Relief	MZW	2	Contract manufacturer	accessdata.fda.gov
Instrument, Ligature Tucking, Orthodontic	ECP	1	Complaint file establishment, Specification developer	accessdata.fda.gov
Instruments, Dental Hand	DZN	1	Contract manufacturer	accessdata.fda.gov
Material, Tooth Shade, Resin	EBF	2	Contract manufacturer, Manufacturer	accessdata.fda.gov
Post, Root Canal	ELR	1	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
August 17, 2015	K151332	Nexus Universal, Nexus Universal Chroma	EMA	Substantially Equivalent	Sybron Dental Specialties	accessdata.fda.gov
August 28, 2000	K001899	IMPROVED TRY-IN GEL	EBF	Substantially Equivalent	Sybron Dental Specialties, Inc.	accessdata.fda.gov
November 9, 1998	K983266	FIBREKOR POST SYSTEM	ELR	Substantially Equivalent	Jeneric/Pentron, Inc.	accessdata.fda.gov
October 30, 1995	K954708	SILANE PRIMER	KLE	Substantially Equivalent	Sybron Dental Specialties, Inc.	accessdata.fda.gov

Compare with other makers

Updated August 17, 2015. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.