Home › Device types › HQP
Unit, Cautery, Thermal, Battery-Powered
FDA product code HQP · Class 2 · Ophthalmic
108
Registered devices
106
Adverse events
3
Recalls
24
510(k) clearances
Devices with this code
Kirwan — KIRWAN SURGICAL PRODUCTS LLCEndo Optiks® — Beaver-Visitec International, Inc.Accu-Temp® — Beaver-Visitec International, Inc.Bovie — ASPEN SURGICAL PRODUCTS, INC.Bovie — ASPEN SURGICAL PRODUCTS, INC.McKesson — MCKESSON MEDICAL-SURGICAL INC.HOTSY — SHIPPERT MEDICAL TECHNOLOGIES, INCBovie — ASPEN SURGICAL PRODUCTS, INC.Endo Optiks® — Beaver-Visitec International, Inc.Endo Optiks® — Beaver-Visitec International, Inc.SUMMIT MEDICAL — Summit Medical, Inc.BVI — Beaver-Visitec International, Inc.CARDINAL HEALTH — Cardinal Health 200, LLCEndo Optiks® — Beaver-Visitec International, Inc.Bovie — ASPEN SURGICAL PRODUCTS, INC.Bovie — ASPEN SURGICAL PRODUCTS, INC.Accu-Temp® — Beaver-Visitec International, Inc.Bovie — ASPEN SURGICAL PRODUCTS, INC.BVI — Beaver-Visitec International, Inc.Bovie — ASPEN SURGICAL PRODUCTS, INC.Inion Cautery — Inion OyBVI — Beaver-Visitec International, Inc.Bovie — ASPEN SURGICAL PRODUCTS, INC.Endo Optiks® — Beaver-Visitec International, Inc.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-07-19 | Beaver Visitec | A small number of devices in this lot may have a melted cap and a hole formed through the packaging. The risk is potentially the product will no longer be steri |
| 2004-06-29 | Aaron Medical Industries, Inc. | The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation. |
| 2004-06-29 | Aaron Medical Industries, Inc. | The cover caps on some of these cauteries are not properly engaged to prevent inadvertent activation. |
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.