Relign Corp

FDA Filings

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

FDA Registration(s)
Registration Number3012790575
FEI Number3012790575
NameRELIGN CORPORATION
Owner & OperatorReLIGN Corporation
Contact Address655 Campbell Technology Parkway, Ste 275
Campbell CA 95008 US
Official Correspondent
  • Nathan Nguyen
  • 01-408-4847599-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address655 Campbell Technology Parkway, Ste 275
Campbell, CA 95008 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
RELIGN CORPORATION
Curved Standard Shaver XL 4.2 mm R-100262022-06-24
RELIGN CORPORATION
Curved Standard Ball Burr XL 5.0 mm R-100252022-06-24
RELIGN CORPORATION
Curved Standard Shaver 3.4mm R-100242021-03-15
RELIGN CORPORATION
Standard Shaver 3.4mm R-100122021-03-15
RELIGN CORPORATION
Standard Burr 5.0mm R-100212020-10-22
RELIGN CORPORATION
Tricera™ Handpiece, Autoclavable R-100232020-08-28
RELIGN CORPORATION
3-in-1 SHAVER™ 4.2mm R-100082020-07-27
RELIGN CORPORATION
Exoflow™ R-100172020-02-28
RELIGN CORPORATION
3-in-1 SHAVER™ 5.0mm R-100142020-02-28
RELIGN CORPORATION
Dynablator™ R-100052020-02-28
RELIGN CORPORATION
Tricera™ Handpiece, Autoclavable R-100112020-02-28
RELIGN CORPORATION
Veriflow™ R-100032020-02-28
RELIGN CORPORATION
Tricera™ Handpiece R-100022020-02-28
RELIGN CORPORATION
Tricera™ Controller R-100012020-02-28
RELIGN CORPORATION
3-in-1 SHAVER™ 5.0mm R-100142019-07-05
RELIGN CORPORATION
Exoflow™ R-100172019-06-20
RELIGN CORPORATION
Veriflow™ R-100032019-04-23
RELIGN CORPORATION
Relign Arthroscopic System2017-01-10
RELIGN CORPORATION
Relign Arthroscopic System2017-01-10
Relign Corporation
Relign System2017-01-04

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