Home › Device types › HDQ
Dilator, Cervical, Fixed Size
FDA product code HDQ · Class 1 · Obstetrics/Gynecology
2,340
Registered devices
12
Adverse events
4
Recalls
6
510(k) clearances
Devices with this code
GEN2 — SURGIX MEDICAL LLCAESCULAP — Aesculap AGIntegra® Miltex® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONNovo Surgical Inc. — NOVO SURGICAL, INC.Hayden Medical — Hayden Medical, Inc.ELMED INCORPORATED — ELMED INCORPORATEDNovo Surgical Inc. — NOVO SURGICAL, INC.Gimmi — Gimmi GmbHMillennium — Avalign Technologies, Inc.Hayden Medical — Hayden Medical, Inc.Quinelato — Schobell Industrial LtdaIntegra® Jarit® — INTEGRA LIFESCIENCES PRODUCTION CORPORATIONSymmetry Surgical® — ASPEN SURGICAL PRODUCTS, INC.BR Surgical, LLC — BR Surgical, LLCELMED — ELMED INCORPORATEDMILLENNIUM — Avalign Technologies, Inc.Millennium — Avalign Technologies, Inc.Millennium — Avalign Technologies, Inc.Marina Medical — MARINA MEDICAL INSTRUMENTS, INC.Hegar Dilator Single Ended — MEDGYN PRODUCTS, INC.Hegar Dilator Single Ended — MEDGYN PRODUCTS, INC.Medicon — Medicon eG. Chirurgiemechaniker-GenossenschaftAmbler Surgical — AMBLER SURGICAL CORP.Symmetry Surgical® — ASPEN SURGICAL PRODUCTS, INC.
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. |
| 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. |
| 2009-04-09 | Marina Medical Instruments Inc. | Marina Medical, Sunrise, FL initiated recall of 46 products of 350 series devices and 47 products of 270 series products because the material used to manufactu |
| 2009-04-09 | Marina Medical Instruments Inc. | Marina Medical, Sunrise, FL initiated recall of 46 different 350 series devices and 47 different 270 series products because the material used to manufacture th |
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