FDA.report

ALPHADENT NV

FDA Registration(s)

RegistrationFEINameStatusInitial importerExpiration yearAddress
80201563006462784ALPHADENT NV1N2020-04-25MANNEBEEKSTRAAT 33 WAREGEM West-Vlaanderen BE 8790

GUDID Contact Samples

Sampled from matched GUDID device records for this company; this is not an exhaustive company contact directory.

Source GUDIDProductPhoneEmail
04260576940049CEKA & PRECI-LINE ATTACHMENTS - Paralleling Mandrel+328004969500info@ckpl.eu
04260576940056CEKA & PRECI-LINE ATTACHMENTS - Orax Standard Rider+328004969500info@ckpl.eu
04260576940063CEKA & PRECI-LINE ATTACHMENTS - Pallax Standard Rider+328004969500info@ckpl.eu

Registered Device Listings

Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
402691031601398K051050SEBOND PINK LIGHT 5G, SEBOND PINK DARK 5G, SEBOND SMART 5ML, SEBOND GRIP 3G, MODELS 644090, 644091, 640066, 644092KLE2005-06-29
402691096479984
402691110961206
402691286152273
402691357877920
402691473331369
402691819949764
402691888245060
402691920142780

Product Codes Associated With Registrations

Product codeRegistration listing recordsLatest decision
KLE12005-06-29

GUDID

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