FDA Device Intelligence
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Set, Anesthesia, Paracervical

FDA product code HEE · Class 2 · Obstetrics/Gynecology

9
Registered devices
15
Adverse events
1
Recalls
9
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-09-01CooperSurgical, Inc.Kit Label incorrect :Labeled with Lidocaine HCI drug cartridges Lidocaine HCl (2%) but contains vials Lidocaine HCl (1%)

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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