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Reherniation Reduction Device

FDA product code QES · Class 3 · Unknown

7

Registered devices

160

Adverse events

1

Recalls

0

510(k) clearances

Devices with this code

Barricaid® ACD (Annular Closure Device) — INTRINSIC THERAPEUTICS, INC.Barricaid® Narrow Anchor ACD - Reusable Instruments Kit — INTRINSIC THERAPEUTICS, INC.Barricaid® Narrow Anchor ACD (Annular Closure Device) — INTRINSIC THERAPEUTICS, INC.Barricaid® Narrow Anchor ACD (Annular Closure Device) — INTRINSIC THERAPEUTICS, INC.Barricaid® ACD (Annular Closure Device) — INTRINSIC THERAPEUTICS, INC.Barricaid® Narrow Anchor ACD Alignment Trial (8mm) — INTRINSIC THERAPEUTICS, INC.Barricaid® Narrow Anchor ACD Alignment Trial (10mm) — INTRINSIC THERAPEUTICS, INC.

Recent recalls

Date	Firm	Reason
2020-07-24	Intrinsic Therapeutics, Inc.	The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BA

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.