ClearanceBrief
Company ยท IT

Thd Spa

FDA 510(k) clearances and medical device recalls filed under this name, 2008 to 2021. Name variants (Inc, Corp, punctuation) are merged.

13510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FERAnoscope And Accessories5
JAFMonitor, Ultrasonic, Nonfetal3
IYOSystem, Imaging, Pulsed Echo, Ultrasonic2
KLAMonitor, Esophageal Motility, Anorectal Motility, And Tube2
FHNLigator, Hemorrhoidal1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 24, 2021K211623THD Procto Software System
Thd Spa, IT
IYO
Jan 26, 2020K193512THD Procto Software System
Thd Spa, IT
IYO
Mar 8, 2018K180135THD Anopress with THD SensyProbe
Thd Spa, IT
KLA
Mar 14, 2017K161785THD ANOPRESS
Thd Spa, IT
KLA
Feb 24, 2015K141657THD REVOLUTION
Thd Spa, IT
JAF
Dec 11, 2013K133687THD N-ANO ANOSCOPE
Thd Spa, IT
FER
Jun 1, 2012K121135THD ANOSCOPE, PROCTOSCOPE, RECTOSCOPE, RECTOSCOPE AND LIGHT-SCOPE
Thd Spa, IT
FER
Mar 1, 2011K103647THD DISPOSABLE ANOSCOPES, PROCTOSCOPES AND RECTOSCOPES
Thd Spa, IT
FER
Jul 15, 2010K093497THD BANDY
Thd Spa, IT
FHN
Jun 11, 2009K091490FAMILY OF THD DISPOSABLE ANOSCOPES/PROCTOSCOPES/RECTOSCOPES
Thd Spa, IT
FER
Jan 28, 2009K090009THD SLIDE ONE
Thd Spa
JAF
Jul 30, 2008K081429THD SLIDE
Thd Spa
JAF
Apr 9, 2008K080132THD DISPOSABLE ANOSCOPE/PROCTOSCOPE
Thd Spa, IT
FER

Latest recalls

DateFirm and productCodeLinked 510(k)
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