Andy Hewes

FDA Filings

This page includes the latest FDA filings for Andy Hewes. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3012523063
FEI Number3012523063
NameAndy Hewes
Owner & Operatorimplantcast
Contact AddressLueneburger Schanze 26
Buxtehude DE-NI Niedersachsen 21614 DE
Official Correspondent
  • Juliane Hoeppner
  • 49-416-1744-135
US Agent
Importing Logistics Registration
Importerimplantcast North America
Address13465 Midway Rd, Ste 310
Dallas, TX 75244 UNITED STATES
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address13465 Midway Rd Ste 310
Dallas, TX 75244 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Andy Hewes [implantcast]
ic-Bipolar Head System2019-08-29
Andy Hewes [implantcast]
ic-Bipolar Head System2019-08-29
Andy Hewes [implantcast]
ic-Bipolar Head System2019-08-29
Andy Hewes [implantcast]
MUTARS Proximal Femur Replacement System2019-03-26
Andy Hewes [implantcast]
MUTARS Proximal Femur Replacement System2019-03-26
Andy Hewes [implantcast]
MUTARS Proximal Femur Replacement System2019-03-26
Andy Hewes [implantcast]
MUTARS torque wrench M8 M102019-03-26
Andy Hewes [implantcast]
MUTARS socket wrench2019-03-26
Andy Hewes [implantcast]
MUTARS engineers wrench SW 242019-03-26
Andy Hewes [implantcast]
Ecofit Hip System2017-10-04

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