Joe Cerami

FDA Filings

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

FDA Registration(s)

• Registration Number: 3007664053
• FEI Number: 3007664053
• Name: Joe Cerami
• Owner & Operator: AprioMed AB
• Contact Address: Virdings alle 28 ; Uppsala SE-C Uppsala lan [SE-03] 754 50 SE
• Official Correspondent:
  • Katrin Svensson
  • 46-18-4301440-x
• US Agent:
  • Joe Cerami
  • AprioMed Inc
  • 978 8288456
  • joe.cerami@apriomed.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 45 South Main St Unit 2 ; Derry, NH 03038 US
• Establishment Type:
  • Develop Specifications But Do Not Manufacture At This Facility
  • Manufacture Medical Device
  • Complaint File Establishment per 21 CFR 820.198

FDA Filings

Device Company	Device	Date
PMN K193268 | KNW Joe Cerami [AprioMed AB]	AprioCore plus	2020-03-05
PMN K181756 | FCG Joe Cerami [AprioMed AB]	Gangi-SoftGuard Coaxial Needle, Gangi-HydroGuard Coaxial Needle	2018-12-27
PMN K150625 | KNW Joe Cerami [AprioMed AB]	Morrison Steerable Needle	2015-07-28
HXY Joe Cerami [AprioMed AB]	Bonopty Adapter	2014-04-16
GDF Joe Cerami [AprioMed AB]	SEESTAR	2005-06-09
GAA Joe Cerami [AprioMed AB]	BONOPTY COAXIAL BONE BIOPSY	2005-03-29

Similar & Related FDA Registered Companies

• AprioMed Inc