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Richard Wolf Medical Instruments Corp.

10 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
E-Line Cutting Electrode 11.5Fr Mono 0 degrees, Sterile. One electrode is placed in a plas recall (Z-1957-2019)Richard Wolf Medical Instruments Corp.2019-06-13
Reuseable rotary blade/abrader, product number 899751305. The round burr is an attachment recall (Z-0789-2016)Richard Wolf Medical Instruments Corp.2016-02-09
Reuseable rotary blade/abrader, product number 899751504. The oval burr laterally hooded i recall (Z-0790-2016)Richard Wolf Medical Instruments Corp.2016-02-09
Reuseable rotary blade/abrader, product number 899751514. The oval burr frontally hooded i recall (Z-0791-2016)Richard Wolf Medical Instruments Corp.2016-02-09
The I-Cart is used to store, transport, and power video equipment used in medical procedur recall (Z-1240-2015)Richard Wolf Medical Instruments Corp.2015-03-03
The Hulka Clip is a sterile packaged medical device that carries a two year expiration dat recall (Z-0037-2015)Richard Wolf Medical Instruments Corp.2014-11-06
Individual units labeled in part: REF: 4630022; for S(a)line resectoscopes; Vaporization e recall (Z-0145-2014)Richard Wolf Medical Instruments Corp.2013-11-04
Richard Wolf Hulka Clip; for single patient use only; a sterile tubal occluding device; 2 recall (Z-0272-2010)Richard Wolf Medical Instruments Corp.2009-11-17
Tubing Set for TEM-Combined System; the tube set consists of a rectal pressure measuring t recall (Z-1430-06)Richard Wolf Medical Instruments Corp.2006-08-24
Pump Tube, REF 8170,121; Suction Pump Drain Tube; An accessory to the suction pump designe recall (Z-0537-04)Richard Wolf Medical Instruments Corp.2004-02-11

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