Stingray Surgical Products

FDA Filings

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

FDA Registration(s)
Registration Number3006059917
FEI Number3006059917
NameSTINGRAY SURGICAL PRODUCTS
Owner & Operatorstingray surgical products
Contact Address156 NW 16th St
Boca Raton FL 33432 US
Official Correspondent
  • mark t mcbrinn
  • x-561-2107582-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address156 NW 16th St
Boca Raton, FL 33432 US
Establishment Type
  • Remanufacture Medical Device
  • Repack or Relabel Medical Device
  • Manufacture Medical Device



FDA Filings

Device
Company
DeviceDate
STINGRAY SURGICAL PRODUCTS
Stingray bipolar forceps2013-08-12
STINGRAY SURGICAL PRODUCTS
Eco-Friendly Forceps2013-08-12
STINGRAY SURGICAL PRODUCTS
STINGRAY BIPOLAR FORCEPS2013-05-10
STINGRAY SURGICAL PRODUCTS
Stingray Leep /Lletz Forceps2011-02-21
STINGRAY SURGICAL PRODUCTS
Stingray Leep/ Lletz Speculum2011-02-21
STINGRAY SURGICAL PRODUCTS
Stingray Instruments2011-02-21
STINGRAY SURGICAL PRODUCTS
Stingray Instrument Trays2011-02-21

Similar & Related FDA Registered Companies

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.