Sendoline Ab

FDA Filings

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

FDA Registration(s)
Registration Number8043690
FEI Number1000629762
NameSENDOLINE AB
Owner & OperatorSENDOLINE AB
Contact AddressMattbandsvagen 12 B BOX 7036
TABY SE-AB Stockholms lan [SE-01] SE-187 66 SE
Official Correspondent
  • Carina - Hjorth
  • 46-8-4458830-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressMattbandsvagen 12 B Box 7036
TABY Stockholms lan [SE-01], SE-187 66 SE
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
SENDOLINE AB
S5 Rotary files starter pack2002-07-26
SENDOLINE AB
S5 Rotary Files2002-07-26
SENDOLINE AB
S5 Retreatment System2002-07-26
SENDOLINE AB
Paste filler2002-07-26
SENDOLINE AB
Big Apical Files2002-07-26
SENDOLINE AB
NiTi Spreader1996-02-20
SENDOLINE AB
Finger Spreader1996-02-20
SENDOLINE AB
S-finder1991-06-21
SENDOLINE AB
S-file1991-06-21

Related Finance Registrations
NCAGE CodeA021NSENDOLINE AB
NCAGE CodeSEJ71SENDOLINE AB
CAGE CodeSEJ71SENDOLINE AB
CAGE CodeA021NSENDOLINE AB
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