Home › Device types › KAM
Cannula, Sinus
FDA product code KAM · Class 1 · General, Plastic Surgery
265
Registered devices
61
Adverse events
2
Recalls
19
510(k) clearances
Devices with this code
Frazier suction tube — Spiggle & Theis Medizintechnik GmbHOSSEOUS — EON MEDITECH PRIVATE LIMITEDOSSEOUS Suction tubes for Nose Reusable — EON MEDITECH PRIVATE LIMITEDReprocessed 4mm EndoScrub Sheath, 30 deg — SURETEK MEDICALEicken antrum cannula — Spiggle & Theis Medizintechnik GmbHFrazier suction tube — Spiggle & Theis Medizintechnik GmbHFrazier suction tube — Spiggle & Theis Medizintechnik GmbHINKA — The Trustee for KAISER FAMILY TRUSTBEAR — Bear-Ent, LLCIntegra® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONJEDMED — JEDMED INSTRUMENT COMPANYEicken antrum cannula — Spiggle & Theis Medizintechnik GmbHBEAR — Bear-Ent, LLCRELIEVA FLEX — ACCLARENT, INC.Instrumentarium — Société Chirurgicale Instrumentarium IncRELIEVA LUMA SENTRY — ACCLARENT, INC.OSSEOUS — EON MEDITECH PRIVATE LIMITEDJEDMED — JEDMED INSTRUMENT COMPANYEicken antrum cannula — Spiggle & Theis Medizintechnik GmbHBEAR — Bear-Ent, LLCOSSEOUS — EON MEDITECH PRIVATE LIMITEDRELIEVA FLEX — ACCLARENT, INC.Reprocessed 4mm EndoScrub Sheath, 70 deg — SURETEK MEDICALMEDLINE — MEDLINE INDUSTRIES, 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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