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Anti Fog Solution And Accessories, Endoscopy
FDA product code OCT · Class 2 · Gastroenterology, Urology
140
Registered devices
181
Adverse events
2
Recalls
27
510(k) clearances
Devices with this code
FloShield/Plus — MINIMALLY INVASIVE DEVICES, INC.FloShield/Plus — MINIMALLY INVASIVE DEVICES, INC.FloShield/Air — MINIMALLY INVASIVE DEVICES, INC.Key Surgical Mr. Clear Anti-Fog — KEY SURGICAL, INC.Merocel® ELVIS® — MEDTRONIC XOMED, INC.FloShield/Plus — MINIMALLY INVASIVE DEVICES, INC.Dr. Fog® Solution With Sponge — ASPEN SURGICAL PRODUCTS, INC.FloShield/Plus — MINIMALLY INVASIVE DEVICES, INC.Plasma Shield — Plasmatica Ltd.ActiFog™ — MEDICAL ACTION INDUSTRIES INC.FloShield/Air — MINIMALLY INVASIVE DEVICES, INC.Robotic FloShield/Plus — MINIMALLY INVASIVE DEVICES, INC.AntiFogOR — THE O R COMPANY PTY LTDMr. Clear Purple — MECTRA LABS, INC.DeRoyal — DEROYAL INDUSTRIES, INC.McKesson — MCKESSON MEDICAL-SURGICAL INC.ClearIt Anti-Fog Cloth — PRESERVATION SOLUTIONS INCFloShield/Plus — MINIMALLY INVASIVE DEVICES, INC.FloShield/Plus — MINIMALLY INVASIVE DEVICES, INC.FloShield/Air — MINIMALLY INVASIVE DEVICES, INC.V. Mueller — STERIS CORPORATIONFloShield/Plus — MINIMALLY INVASIVE DEVICES, INC.FloShield/Air — MINIMALLY INVASIVE DEVICES, INC.FloShield/Air — MINIMALLY INVASIVE DEVICES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-01-14 | Sunstar Americas, Inc. | Product lacks premarket clearance. |
| 2019-05-30 | Medline Industries, Inc. | The Anti-Fog Solution may not defog properly due to a degradation in the chemical properties. |
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