Ackermann Usa

FDA Filings

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

Ackermann Usa holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number3009319607
FEI Number3009319607
NameACKERMANN USA INC
Owner & OperatorAckermann USA
Contact Address592 Middle Road
Bayport NY 11705 US
Official Correspondent
  • Richard Rodgers
  • x-631-8683886-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address592 MIDDLE RD
Bayport, NY 11705 US
Establishment TypeRepack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
ACKERMANN USA INC [Ackermann USA]
arthroscopic accessories2019-05-29
ACKERMANN USA INC [Ackermann USA]
surgical punch2019-05-29
ACKERMANN USA INC [Ackermann USA]
hemostatic clip applier2019-05-29
ACKERMANN USA INC [Ackermann USA]
EasyAngle2019-05-23

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