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Cannula, Sinus
FDA product code KAM · Class 1 · General, Plastic Surgery
266
Registered devices
61
Adverse events
2
Recalls
19
510(k) clearances
Devices with this code
BEAR — Bear-Ent, LLCBEAR — Bear-Ent, LLCMSI Precision Specialty Instruments — Med Saver, Inc.Frazier suction tube — Spiggle & Theis Medizintechnik GmbHEicken antrum cannula — Spiggle & Theis Medizintechnik GmbHOSSEOUS — EON MEDITECH PRIVATE LIMITEDBEAR — Bear-Ent, LLCEicken antrum cannula — Spiggle & Theis Medizintechnik GmbHOSSEOUS Suction tubes for Nose Reusable — EON MEDITECH PRIVATE LIMITEDFrazier suction tube — Spiggle & Theis Medizintechnik GmbHOSSEOUS Suction tubes for Nose Reusable — EON MEDITECH PRIVATE LIMITEDEicken antrum cannula — Spiggle & Theis Medizintechnik GmbHOSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS — EON MEDITECH PRIVATE LIMITEDSuction- / Irrigation tube — Spiggle & Theis Medizintechnik GmbHEicken antrum cannula — Spiggle & Theis Medizintechnik GmbHBEAR — Bear-Ent, LLCOSSEOUS — EON MEDITECH PRIVATE LIMITEDIntegra® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONSuction tube with interruptor, tip — Spiggle & Theis Medizintechnik GmbHINKA — The Trustee for KAISER FAMILY TRUSTFrazier suction tube — Spiggle & Theis Medizintechnik GmbHRELIEVA FLEX — ACCLARENT, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2015-04-28 | Acclarent, Inc. | Acclarent determined that one single RELIEVA FLEX Sinus Guide Catheter was distributed past it's expiry date. |
| 2013-05-03 | Surgical Instrument Service And Savings, Inc. | The seal which maintains a sterile barrier for reprocessed medical devices became compromised to the point where product may fall out of the pouch. |
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