Data / Medical devices / United States / Kerr Corporation
Kerr Corporation: FDA-registered device maker in Pomona, CA, United States, 50 510(k) clearances
Kerr Corporation is registered with the FDA (registration 3012477813) in Pomona, CA, United States. It lists 65 device types. The FDA files 50 510(k) clearances under its listings, the newest dated January 7, 2026. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3012477813
- Address
- 1889 W Mission Blvd, Pomona, CA, United States, 91766
- Owner or operator
- SYBRON DENTAL SPECIALTIES, INC. (9029565)
- Roles
- Complaint file establishment, Contract manufacturer, Manufacturer, Repackager or relabeler, Reprocessor, Specification developer
- First device listed
- December 15, 1977
- Registered through
- 2027
- Brand names listed
- ALLRAP CHAIR SLEEVE FULL SNG4556-75C, ALLRAP/SLIP-N-GRIP, AP SLIP-N-GRIP SLEEVE UNIVERSAL SNG2980-75C, AXIS Laminate Veneer Set, Acrylic Adjustment Logic Set, AlgiNot, All Ceramic Logic Set, All-Purpose Esthetic Logic Set and more
Devices it lists
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 |
|---|---|---|---|---|---|---|
| January 7, 2026 | K252890 | ZenSeal Pro | KIF | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| October 14, 2025 | K253461 | Demi Pro | EBZ | Substantially Equivalent | Meta Systems Co., Ltd. | accessdata.fda.gov |
| January 12, 2023 | K222830 | Rainbow 360 | KLE | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| August 31, 2022 | K221255 | SimpliShade Bulk Fill, SimpliShade Bulk Fill Flow | EBF | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| October 11, 2019 | K191548 | Nexus Universal Self-Cure | EMA | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| August 8, 2017 | K162948 | Styptin, Hemogin-L, Hemodettes, and GingiGEL Aluminum Chloride Impregnated Retraction Cord/Materials | MVL | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| April 28, 2017 | K162258 | Self Sealing Sterilization Pouches | FRG | Substantially Equivalent | Tianchang Jiarui Packaging Material Co., Ltd. | accessdata.fda.gov |
| March 17, 2017 | K163239 | SMARTmatic | EFA | Substantially Equivalent | Kaltenbach & Voigt GmbH | accessdata.fda.gov |
| February 21, 2017 | K163317 | ELECTROmatic | EBW | Substantially Equivalent | Kaltenbach & Voigt Gmgh | accessdata.fda.gov |
| November 7, 2016 | K162257 | P1145 Dental Restorative | EBF | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| February 5, 2015 | K143209 | SonicFill 2 | EBF | Substantially Equivalent | Sybron Dental Specialties | accessdata.fda.gov |
| July 2, 2014 | K140685 | ENDO VAC APICAL NEGATIVE PRESSURE IRIGATION SYSTEM | NYL | Substantially Equivalent | Sybron Endo | accessdata.fda.gov |
| May 30, 2013 | K130869 | TAKE 1 ADVANCE | ELW | Substantially Equivalent | Sybron Dental Specialties | accessdata.fda.gov |
| February 19, 2013 | K123595 | NEXUS RMGI | EMA | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| April 26, 2012 | K112153 | IROOT 100 MINI | LQY | Substantially Equivalent | S-Denti Co., Ltd. | accessdata.fda.gov |
| April 20, 2012 | K120037 | BLUWHITE DIAMOND DENTAL BURS MODIFIED | DZP | Substantially Equivalent | Beavers Dental, Div. Sybron Canada, Ltd. | accessdata.fda.gov |
| April 8, 2011 | K110092 | TAKE 1 ADVANCED RIGID TRAY | ELW | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| January 20, 2011 | K103351 | DMC COMPOSITE 2 | EBF | Substantially Equivalent | Kerr Corporation | accessdata.fda.gov |
| April 3, 2009 | K090292 | PREMISE MODIFIED | EBF | Substantially Equivalent | Kerr Corp. | accessdata.fda.gov |
| December 11, 2008 | K082671 | HERCULITE ULTRA | EBF | Substantially Equivalent | Sybron Dental Specialties | accessdata.fda.gov |
| August 29, 2008 | K081887 | LUTE-IT II VENEER CEMENT, MODEL NO6 | EMA | Substantially Equivalent | Pentron Clinical Technologies | accessdata.fda.gov |
| August 3, 2006 | K061230 | VECTORS TEMPORARY ANCHORAGE SYSTEM | OAT | Substantially Equivalent | Sybron Dental Specialties | accessdata.fda.gov |
| February 3, 2006 | K053565 | TEMPBOND CLEAR WITH TRICLOSAN | EMA | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| April 15, 2005 | K050604 | KERR VPS IMPRESSION MATERIAL | ELW | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| April 28, 2004 | K031664 | ELEMENTS OBTURATION UNIT | EKR | Substantially Equivalent | Sybron Endo/Analytic | accessdata.fda.gov |
| March 5, 2003 | K024198 | SMEARCLEAR | KJJ | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| July 5, 2002 | K021253 | ULTRASONIC TIPS WITH DIAMOND COATING | ELC | Substantially Equivalent | Sybron Endo/Analytic | accessdata.fda.gov |
| April 22, 2002 | K020555 | SONATA MICRO HYBRID COMPOSITE | EBF | Substantially Equivalent | Pentron Laboratory Technologies | accessdata.fda.gov |
| September 4, 2001 | K012405 | EXTRUDE MODIFIED | ELW | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| April 23, 2001 | K010994 | TAKE ONE BITE MODIFIED | ELW | Substantially Equivalent | Kerr Corp. | accessdata.fda.gov |
| February 15, 2001 | K003650 | PERMLASTIC 3 | ELW | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| January 4, 2001 | K003658 | TEMP-BOND NE 2 | EMA | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| August 28, 2000 | K001899 | IMPROVED TRY-IN GEL | EBF | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| July 5, 2000 | K001218 | CORRECT PLUS | ELW | Substantially Equivalent | Jeneric/Pentron, Inc. | accessdata.fda.gov |
| February 29, 2000 | K000173 | CEMENT IT! UNIVERSAL C&B | EMA | Substantially Equivalent | Jeneric/Pentron, Inc. | accessdata.fda.gov |
| October 14, 1999 | K992484 | RCNG: ROOT CANAL NEGOTIATING GEL; MODEL RCNG | KJJ | Substantially Equivalent | Jordco, Inc. | accessdata.fda.gov |
| November 9, 1998 | K983266 | FIBREKOR POST SYSTEM | ELR | Substantially Equivalent | Jeneric/Pentron, Inc. | accessdata.fda.gov |
| April 7, 1997 | K970715 | SYSTEM B HEAT SOURCE | EAT | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| January 30, 1997 | K962288 | COVER-ALL, DRAPE-IT-ALL, CHAIR SLEVE, X-RAY SLEEVE, HEADREST COVER | MMP | Substantially Equivalent | Pinnacle Products, Inc. | accessdata.fda.gov |
| December 2, 1996 | K963862 | TOUCH N' HEAT | EAT | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| September 12, 1996 | K962540 | E-TYPE CONTRA ANGLE NAC-E | EGS | Substantially Equivalent | Nsk Nakanishi, Inc. | accessdata.fda.gov |
| March 11, 1996 | K955932 | EXAFLEX IMPRESSION MATERIAL (MODIFICATION) | ELW | Substantially Equivalent | GC America, Inc. | accessdata.fda.gov |
| February 21, 1996 | K960352 | ALLRAP/SLIP-N-GRIP | EFB | Substantially Equivalent | Dental Disposables Intl., Inc. | accessdata.fda.gov |
| November 17, 1994 | K943642 | HERCULITE XR & XRV | EBF | Substantially Equivalent | Sybron Dental Specialties, Inc. | accessdata.fda.gov |
| February 14, 1994 | K934714 | ENDODONTIC PULP CANAL SPREADER | ELC | Substantially Equivalent | Excellence IN Endodontics, Inc. | accessdata.fda.gov |
| April 28, 1992 | K914178 | CORRECTED-V.P.S. | ELW | Substantially Equivalent | Jeneric/Pentron, Inc. | accessdata.fda.gov |
| September 6, 1990 | K902646 | HOOD GEAR (TM) BREAKAWAY HEADGEAR WITH NECK STRAP | DZB | Substantially Equivalent | Ormco Corp. | accessdata.fda.gov |
| September 6, 1990 | K902645 | HOOD GEAR (TM) BREAKAWAY HEADGEAR W/ HIGH PULL | DZB | Substantially Equivalent | Ormco Corp. | accessdata.fda.gov |
| October 25, 1984 | K843023 | KERR PORCELAIN REPAIR PRIMER | KLE | Substantially Equivalent | Kerr Corporation (Danbury) | accessdata.fda.gov |
| April 14, 1981 | K810825 | POLYVINYL SILICONE IMPRESSION MATERIAL | ELW | Substantially Equivalent | Dental-Material Gesellschaft | accessdata.fda.gov |
Compare with other makers
- All makers of Cleanser, Root Canal
- All makers of Material, Tooth Shade, Resin
- All makers of Cement, Dental
- All makers of Implant, Endosseous, Orthodontic
- All makers of Headgear, Extraoral, Orthodontic
- All makers of Accessories, Implant, Dental, Endosseous
Updated January 7, 2026. 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.