Kerr Corporation (Danbury)
Orange, CA, US
Kerr Corporation (Danbury) appears in FDA device records in Orange, CA. FDA records list 32 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 32
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 32 510(k) clearances for Kerr Corporation (Danbury) between 1978 and 2005. The busiest year on record is 1984, with 6. The most recent is 2005, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1978 | 5 |
| 1984 | 6 |
| 1985 | 1 |
| 1986 | 2 |
| 1987 | 1 |
| 1988 | 4 |
| 1989 | 1 |
| 1990 | 1 |
| 1991 | 1 |
| 1992 | 2 |
| 1993 | 1 |
| 1994 | 2 |
| 1995 | 3 |
| 2002 | 1 |
| 2005 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K051545 | L.E. DEMETRON II | EBZ | Substantially Equivalent | |
| K020091 | OPTILUX 501 | EBZ | Substantially Equivalent | |
| K951663 | TYTIN R | EJJ | Substantially Equivalent | |
| K951511 | TYTIN ADMIX | EJJ | Substantially Equivalent | |
| K942480 | M4 CONTRA-ANGLE HANDPIECE | EGS | Substantially Equivalent | |
| K940513 | OPTIBOND | KLE | Substantially Equivalent | |
| K935535 | TYTIN | EJJ | Substantially Equivalent | |
| K934690 | KERR OPTIBOND, MODIFICATION | KLE | Substantially Equivalent | |
| K923546 | OPTIBOND | KLE | Substantially Equivalent | |
| K915847 | AUTOMIX DENTAL AMALGAMATOR | EFD | Substantially Equivalent | |
| K904756 | MATRICS | ESD | Substantially Equivalent | |
| K904482 | STAT.BR TM | ELW | Substantially Equivalent | |
| K894219 | TEMP BOND NE | EMA | Substantially Equivalent | |
| K880251 | KERR XR IONOMER | EMA | Substantially Equivalent | |
| K880250 | KERR XR BOND | EMA | Substantially Equivalent | |
| K880685 | PORCELITE DUAL CURE CEMENT | EMA | Substantially Equivalent | |
| K880684 | XR PRIMER | KLE | Substantially Equivalent | |
| K872147 | KERR CAVALITE | EJK | Substantially Equivalent | |
| K860346 | KERR PORCELITE | KLE | Substantially Equivalent | |
| K860532 | KERR POL-E-LASTIC DENTAL IMPRESSION MATERIAL | ELW | Substantially Equivalent | |
| K844662 | KERR HERCULITE DENTAL COMPOSITE RESTORATIVE MATERI | EBF | Substantially Equivalent | |
| K843025 | COMMAND ENAMEL-DENT DENTAL ADHESIVE | KLE | Substantially Equivalent | |
| K843023 | KERR PORCELAIN REPAIR PRIMER | KLE | Substantially Equivalent | |
| K843026 | KERR GELLED PHOSPHORIC ACID ETCHANT | EBF | Substantially Equivalent | |
| K843024 | COMMAND ULTRASEAL PIT & FISSURE SEALANT | EBC | Substantially Equivalent | |
| K843072 | EVER-BOND V GLASS LONOMER RESTORATIVE | EBF | Substantially Equivalent | |
| K843022 | KERR COMMAND ULTRAFINE POLISHING PASTE | EJR | Substantially Equivalent | |
| K781688 | LINER, CAVITY CALCIUM HYDROXIDE | EJK | Substantially Equivalent | |
| K781689 | REFLECT IMPRESSION MATERIAL | ELW | Substantially Equivalent | |
| K780712 | KERR DISCOVERY DISPOSABLE FLUORIDE TRAY | KMT | Substantially Equivalent | |
| K780213 | HANDPIECE, LIFT, ENDO | EGS | Substantially Equivalent | |
| K780211 | 4-IN-1 DISP. CROWN & BRIDGE TRAY | EHY | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- EBZActivator, Ultraviolet, For Polymerization
- EJRAgent, Polishing, Abrasive, Oral Cavity
- KLEAgent, Tooth Bonding, Resin
- EJJAlloy, Amalgam
- EFDAmalgamator, Dental, Ac-Powered
- EMACement, Dental
- EGSHandpiece, Contra- And Right-Angle Attachment, Dental
- ESDHearing Aid, Air-Conduction, Prescription
- EJKLiner, Cavity, Calcium Hydroxide
- ELWMaterial, Impression
- EBFMaterial, Tooth Shade, Resin
- EBCSealant, Pit And Fissure, And Conditioner
- KMTTray, Fluoride, Disposable
- EHYTray, Impression, Preformed
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain