FDA 510(k)

Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono

Numéro K : K171562 · 2018-04-13

Date de décision2018-04-13

Code produitELW

Comité consultatifDE

DécisionSubstantially Equivalent

Résumé du dispositif

Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono is the device name listed in this FDA 510(k) record. The listed applicant is Dreve Dentamid GmbH. It received FDA 510(k) clearance on 2018-04-13 under 510(k) number K171562. The device is classified under product code ELW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono?

Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono is a medical device that received FDA 510(k) clearance on 2018-04-13. The listed applicant is Dreve Dentamid GmbH. The 510(k) number is K171562.

When did Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono receive FDA 510(k) clearance?

Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono received FDA 510(k) clearance on 2018-04-13, under 510(k) number K171562.

Who is the listed applicant for Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono?

The FDA 510(k) record lists Dreve Dentamid GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono?

The FDA product code for Dynax clear, Dynax putty, Dynax heavy body, Dynax light, Dynax mono is ELW.

Essais cliniques associés

Les enregistrements connexes sont mis en correspondance automatiquement à l'aide des noms, codes produits ou autres métadonnées. Une mise en correspondance n'établit pas de relation clinique, scientifique, corporative ou réglementaire vérifiée ; veuillez consulter les sources officielles liées.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Autres dossiers indiquant Dreve Dentamid GmbH en tant que demandeur

K250739Primeprint Direct Aligner K200580FotoDent denture K190571StoneBite and StoneBite scan K162408Nano Varnish, Plaquit, Lightpaint on Surface K171729Fixtemp C&B

Dispositifs connexes (Code : ELW)

K254152Dia-X Sil Light BodyDiaDent Group International K254142Dia-X Sil Heavy BodyDiaDent Group International K254112Dia-X Sil BiteDiaDent Group International K253501Hydro Print Premium Fast Set - 454g (1lb) (052037); Hydro Print Premium Regular Set - 454g (1lb) (052327); Chroma Print Premium Fast Set - 454g (1lb) (052457); Chroma Print Premium Regular Set - 454g (1lb) (051460); Perfil Pro - 454g (1lb) (056213); Perfil Pro+ - 454g (1lb) (056121); Perfil Pro Chroma - 454g (1lb) (056122); Hydro Print Premium Fast Set - Multi Pack (056205); Hydro Print Premium Regular Set - Multi Pack (056208); Hydro Print Premium Fast Set - 9,07Kg (20lb) (056204);Vigodent Indústria E Comercio Ltda K250969JET BITE; JET BLUE BITE FAST; JET BLUE BITE SUPERFASTDent4you AG K241924Elastic Impression MaterialBeijing Okvd Biological Technology , Ltd.

Source officielle

Voir dans la base de données FDA →

Données issues de l'API ouverte de la FDA. Pour les informations les plus récentes et faisant autorité, veuillez toujours vous référer au registre officiel.