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NLX
NAKANISHI INC. · Model NLX CD · UDI-DI 04560264572829
EBW
Prescription
10
510(k) clearances
392
Adverse events
2
Recalls
69
Facilities
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2017-12-21 | W & H DentalWerk Burmoos GMBH - Site 1 | During continuous postmarket surveillance activities, we have noticed a potential malfunction of individual foot controls of the type S-N1/S-N2. In case the error occurs, the foot |
| 2013-10-24 | Nobel Biocare Usa Llc | The recall was initiated because there is a potential for malfunction of the OsseoCare Pro when used with the OseeoCare Pro iPad application software release 1.2.0.7. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.