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Kensey Nash Corp

12 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
a translucent, rectangular, resorbable, collagen membrane sheet derived from bovine tissue recall (Z-1621-2012)Kensey Nash Corp2012-05-17
a translucent, rectangular, resorbable, collagen membrane sheet derived from bovine tissue recall (Z-1622-2012)Kensey Nash Corp2012-05-17
a translucent, rectangular, resorbable, collagen membrane sheet derived from bovine tissue recall (Z-1623-2012)Kensey Nash Corp2012-05-17
ThromCat Thrombectomy Catheter System. Catalog number 63000-01 recall (Z-1115-2007)Kensey Nash Corp2007-07-23
TriActiv FX Embolic Protection System 7F, Catalog numbers 60040-02 (has 190 cm guidewire) recall (Z-0833-2007)Kensey Nash Corp2007-05-31
FX Spare Shieldwire Inflators (3.0 - 5.0 mm), Catalog number 60042-02. The product is sold recall (Z-0834-2007)Kensey Nash Corp2007-05-31
ProGuard Spare Shieldwire Inflators (2.5 - 5.0 mm), Catalog number 61030-01. The product i recall (Z-0835-2007)Kensey Nash Corp2007-05-31
ThromCat Thrombectomy Catheter System. 7F 2.5 -7.0 mm 150 cm. Catalogue number 63000-01. I recall (Z-0597-2007)Kensey Nash Corp2007-03-08
TriActiv ProGuard Embolic Protection System, Part number 61000-01. The product is shipped recall (Z-1305-06)Kensey Nash Corp2006-07-28
TriActiv System Procedure Kit. Balloon Protected Flush Extraction System 190 cm (for embol recall (Z-1219-06)Kensey Nash Corp2006-07-12
TriActiv System Procedure Kit. Balloon Protected Flush Extraction System 340 cm (for embol recall (Z-1220-06)Kensey Nash Corp2006-07-12
TriActiv System Balloon Inflation Syringe. The syringe packs/boxes contain 5 'spare' syrin recall (Z-1221-06)Kensey Nash Corp2006-07-12

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Every clearance here is in the API, with alerts when new ones post.