Noritake Co., Inc.
Washington, DC, US
Noritake Co., Inc. appears in FDA device records in Washington, DC. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Noritake Co., Inc. between 1989 and 2011. The busiest year on record is 2005, with 4. The most recent is 2011, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1989 | 1 |
| 1998 | 3 |
| 1999 | 2 |
| 2003 | 2 |
| 2005 | 4 |
| 2011 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K111383 | ZIRPRIME | EIH | Substantially Equivalent | |
| K111107 | SUPER PORCELAIN EX-3 UNIVERSAL OPAQUE | EIH | Substantially Equivalent | |
| K052304 | SUPER PORCELAIN EX-3 PRESS | EIH | Substantially Equivalent | |
| K050920 | CZR PRESS LF STAINS | EIH | Substantially Equivalent | |
| K050160 | KATANA ZIRCONIA | EIH | Substantially Equivalent | |
| K043462 | CZR PRESS LF | EIH | Substantially Equivalent | |
| K031968 | CERABIEN ZR | EIH | Substantially Equivalent | |
| K033049 | CZR PRESS | EIH | Substantially Equivalent | |
| K992023 | GRAND CERAM | EIH | Substantially Equivalent | |
| K992024 | SUPER PORCELAIN TI-22 | EIH | Substantially Equivalent | |
| K983470 | SUPER PORCELAIN STAIN- PURE WHITE | EIH | Substantially Equivalent | |
| K983247 | SUPER PORCELAIN ADDMATE | EIH | Substantially Equivalent | |
| K982766 | PASTE OPAQUE EX-3 | EIH | Substantially Equivalent | |
| K884356 | NORITAKE SUPER PORCELAIN EX-3 | EIH | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
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
