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Remover, Intrauterine Device, Contraceptive, Hook-Type
FDA product code HHF · Class 1 · Obstetrics/Gynecology
47
Registered devices
3
Adverse events
1
Recalls
6
510(k) clearances
Devices with this code
Hayden Medical — Hayden Medical, Inc.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Gynex — GYNEX CORPORATIONHNM MEDICAL — HNM STAINLESS, LLC.Gynex — GYNEX CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONEOS — NORTH EOS INDUSTRIES INC.MSI Precision Specialty Instruments — Med Saver, Inc.AESCULAP — Aesculap AGBR Surgical, LLC — BR Surgical, LLCDouble IUD Extractor — Coopersurgical, Inc.Gynex — GYNEX CORPORATIONPILLING — TELEFLEX INCORPORATEDIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONV. Mueller — STERIS CORPORATIONNA — PANPAC MEDICAL CORPORATIONGynex — GYNEX CORPORATIONNovo Surgical Inc. — NOVO SURGICAL, INC.BR Surgical, LLC — BR Surgical, LLCNovo Surgical — NOVO SURGICAL, INC.Novo Surgical — NOVO SURGICAL, INC.MEDLINE INDUSTRIES, INC. — MEDLINE INDUSTRIES, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.HNM MEDICAL — HNM STAINLESS, LLC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2024-12-03 | Sklar Instruments | Reports of various packaging issues that may result in a breach of the sterile barrier. |
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