Coracoid Solutions L L C

FDA Filings

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

FDA Registration(s)
Registration Number3014020962
FEI Number3014020962
NameCORACOID SOLUTIONS, LLC.
Owner & OperatorCoracoid Solutions, LLC.
Contact Address661 Live Oak Ave. Suite 3
Menlo Park CA 94025 US
Official Correspondent
  • Steven Golden
  • x-650-7400306-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address661 Live Oak Ave. Suite 3
Menlo Park, CA 94025 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device
Company
DeviceDate
CORACOID SOLUTIONS LLC
 J-Pass Suture Passer 2020-02-06
CORACOID SOLUTIONS LLC
 M-Fix 7mm 2018-07-19
CORACOID SOLUTIONS LLC
 M-Fix 4mm 2018-07-19
CORACOID SOLUTIONS, LLC.
M-Fix Acromioclavicular2017-10-04
CORACOID SOLUTIONS, LLC.
J-Pass Passing Device2017-10-04

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