Dannik

FDA Filings

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

FDA Registration(s)
Registration Number3015775837
FEI Number3015775837
NameDANNIK
Owner & OperatorDANNIK
Contact Address941 W Morse Blvd. Suite 100
Winter Park FL 32789 US
Official Correspondent
  • Olga Haberland
  • 1-407-7451698-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address941 W Morse Blvd. Suite 100
Winter Park, FL 32789 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
Dannik
DANNIK Disposable Monopolar Laparoscopic Instrument2020-06-09
DANNIK
DANNIK Specimen Retrieval System With Deployment Mechanism, DANNIK Specimen Retrieval System (Bag Only)2020-04-21
DANNIK
DANNIK Disposable Monopolar Instruments2020-03-09
Dannik
DANNIK Disposable Monopolar Laparoscopic Instrument2020-03-04
DANNIK
SURGICAL CLIP APPLIER2020-01-20
DANNIK
Dannik Titanium Ligation Clip2020-01-13
DANNIK
Trocar Cannula System2020-01-13
Dannik
Dannik Titanium Ligation Clip2019-12-20
DANNIK
GRAVITY SUCTION IRRIGATION2019-12-18
Dannik
Dannik Laparoscopic Suction Irrigation System2019-11-19

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