ClearanceBrief
Company ยท US

Spintech, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 2022. Name variants (Inc, Corp, punctuation) are merged.

12510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
EJISyringe, Cartridge3
LNHSystem, Nuclear Magnetic Resonance Imaging3
FMFSyringe, Piston2
FXXMask, Surgical2
EFBHandpiece, Air-Powered, Dental1
KWPAppliance, Fixation, Spinal Interlaminal1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Oct 28, 2022K223079Stage
Spintech, Inc.
LNH
Nov 14, 2021K212109Spin Care Disposable Protective Mask Level 3
Spintech, LLC
FXX
Jun 29, 2021K210843STAGE
Spintech, Inc.
LNH
Mar 18, 2021K201624Spin Care Disposable Protective Mask
Spintech, LLC
FXX
Feb 23, 2018K173224SPIN-SWI
Spintech, Inc.
LNH
Sep 2, 2003K023722SAFETYWAND DISPOSABLE HANDPIECE
Spintech, Inc.
EJI
Jun 29, 2001K010692THE WAND PLUS COMPUTER CONTROLLED ANESTHETIC DELIVERY SYSTEM
Spintech, Inc.
FMF
Jun 6, 2000K992404THE WAND
Spintech, Inc.
FMF
May 11, 2000K992819WAND PLUS
Spintech, Inc.
EJI
Jul 5, 1996K961648THE WAND
Spintech, Inc.
EJI
Feb 8, 1996K955654SHORTSTOP DISPOSABLE PROPHY ANGLE
Spintech, Inc.
EFB
Dec 23, 1992K922238LEAPLAZA FRAME
Spintech, Inc.
KWP

Latest recalls

DateFirm and productCodeLinked 510(k)
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