Company ยท FR
Moria SA
FDA 510(k) clearances and medical device recalls filed under this name, 1998 to 2017. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 26, 2017 | K172994 | EPI K Console Moria SA, FR | HNO |
| Mar 25, 2005 | K043183 | EPI-K Moria SA, FR | HNO |
| Jun 18, 2004 | K032836 | M3 MICROKERATOME Moria SA, FR | HNO |
| Mar 31, 2004 | K040297 | ONEUSE- PLUS MICROKERATOME Moria SA, FR | HMY |
| Sep 27, 2002 | K022560 | M2 SINGLE USE MICROKERTOME Moria SA, FR | HMY |
| Mar 9, 2001 | K003594 | CARRIAZO BARRAQUER SINGLE USE MICROKERATOME Moria, Inc., FR | HMY |
| Oct 12, 2000 | K002191 | CARRIAZO BARRAQUER II MICROKERATOME Moria, Inc., FR | HMY |
| Aug 25, 1998 | K981742 | ONE UP DISPOSABLE KERATOME HEAD Moria, Inc., FR | HNO |
| Jul 24, 1998 | K981741 | CARRIAZO BARRAQUER MICROKERATOME Moria, Inc., FR | HMY |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||