Home › Device types › HHF
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
Gynex — GYNEX CORPORATIONGynex — GYNEX CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONAESCULAP — Aesculap AGNovo Surgical — NOVO SURGICAL, INC.Symmetry Surgical — ASPEN SURGICAL PRODUCTS, INC.BR Surgical, LLC — BR Surgical, LLCBR Surgical, LLC — BR Surgical, LLCBR Surgical, LLC — BR Surgical, LLCHNM MEDICAL — HNM STAINLESS, LLC.Symmetry Berke-Jaeger — ASPEN SURGICAL PRODUCTS, INC.Novo Surgical Inc. — NOVO SURGICAL, INC.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Avalign — Avalign Technologies, Inc.Instrapac — ROBINSON HEALTHCARE LIMITEDNovo Surgical Inc. — NOVO SURGICAL, INC.Novo Surgical — NOVO SURGICAL, INC.HNM MEDICAL — HNM STAINLESS, LLC.HNM MEDICAL — HNM STAINLESS, LLC.MEDLINE INDUSTRIES, INC. — MEDLINE INDUSTRIES, INC.V. Mueller — STERIS CORPORATIONHayden Medical — Hayden Medical, Inc.HNM MEDICAL — HNM STAINLESS, LLC.Integra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATION
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. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.