FDA Device Intelligence
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Transurethral Occlusion Insert, Urinary Incontinence-Control, Female

FDA product code OCK · Class 3 · Unknown

7
Registered devices
7
Adverse events
8
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2010-04-27Rochester Medical CorpRochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a smal
2010-04-27Rochester Medical CorpRochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a smal
2010-04-27Rochester Medical CorpRochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a smal
2010-04-27Rochester Medical CorpRochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a smal
2010-04-27Rochester Medical CorpRochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a smal
2010-04-27Rochester Medical CorpRochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a smal
2010-04-27Rochester Medical CorpRochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a smal
2010-04-27Rochester Medical CorpRochester Medical is voluntarily recalling specific lots of FemSoft urethral inserts manufactured and distributed in 2009 and 2010. Testing has revealed a smal

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.