Home › Device types › HHK
Curette, Suction, Endometrial (And Accessories)
FDA product code HHK · Class 2 · Obstetrics/Gynecology
149
Registered devices
60
Adverse events
3
Recalls
42
510(k) clearances
Devices with this code
VACURETTE — Gyrus ACMI, LLCCombo-Pak — Coopersurgical, Inc.Cannula-Curette — Coopersurgical, Inc.NA — PANPAC MEDICAL CORPORATIONCrossGlide — CROSS BAY MEDICAL, INC.Uterine Explora Curette - Model I — Coopersurgical, Inc.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONCannula-Curette — Coopersurgical, Inc.Cannula-Curette — Coopersurgical, Inc.Tis-U-Trap Uterine Suction Curette Set — Coopersurgical, Inc.Premier — PREMIER DENTAL PRODUCTS COMPANYCannula-Curette — Coopersurgical, Inc.Gyrus ACMI — Gyrus ACMI, LLCCannula-Curette — Coopersurgical, Inc.Cannula-Curette — Coopersurgical, Inc.Pipet Curet — Coopersurgical, Inc.Tis-U-Trap Uterine Suction Curette Set — Coopersurgical, Inc.Tis-U-Trap Uterine Suction Curette Set — Coopersurgical, Inc.V. Mueller — CAREFUSION 2200, INCBerkeley Vacurette — Gyrus ACMI, LLCTis-U-Trap Uterine Suction Curette Set — Coopersurgical, Inc.Suresample, Endometrial Sampler — GYNEX CORPORATIONNA — PANPAC MEDICAL CORPORATIONGyrus ACMI — Gyrus ACMI, LLC
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-09-16 | Olympus Corporation of the Americas | Update to the Instruction for Use (IFU): Olympus is adding a new warning against the use of accessories which are not listed in the IFU. There have been reporte |
| 2014-10-27 | CooperSurgical, Inc. | The product has been identified to contain an incorrect curette type. |
| 2014-09-08 | Instrumed International, Inc. | The reason these devices are being withdrawn from the market by Instrumed is that Instrumed did not market these devices prior to September 26, 1976, and theref |
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