Home › Device types › HRQ
Hemostat
FDA product code HRQ · Class 1 · General, Plastic Surgery
2,232
Registered devices
93
Adverse events
3
Recalls
15
510(k) clearances
Devices with this code
Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftMedicon — Medicon eG. Chirurgiemechaniker-GenossenschaftIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONPILLING — TELEFLEX INCORPORATEDIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATIONSymmetry Surgical® — ASPEN SURGICAL PRODUCTS, INC.AESCULAP — Aesculap AGHayden Medical — Hayden Medical, Inc.AESCULAP — AESCULAP, INC.Integra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONHELMUT ZEPF — Helmut Zepf Medizintechnik GmbHCARDINAL HEALTH — Cardinal Health 200, LLCBR Surgical, LLC — BR Surgical, LLCBOSS Instruments — BOSS INSTRUMENTS, LTD., INC.Gill — The Radebaugh-Fetzer CompanyASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATIONIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONHayden Medical — Hayden Medical, Inc.BOSS Instruments — BOSS INSTRUMENTS, LTD., INC.STOMA® — Storz am Mark GmbHASSI — ACCURATE SURGICAL & SCIENTIFIC INSTRUMENTS CORPORATION
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2025-01-31 | Aesculap Inc | The forceps have been used in ways not covered by the design resulting in breakage of the clamps. |
| 2024-11-12 | MEDLINE INDUSTRIES, LP - Northfield | Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection. |
| 2024-02-23 | MEDLINE INDUSTRIES, LP - Northfield | Product may have a weak seal which may result in a breach of sterility of the contents if the seal fails. The weak seal may not be detectable by all users. |
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