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Adiana Permanent Contraception System

by Hologic, Inc.

PMA P070022

Active United States

PMA

Valid until

No expiry

PMA approval is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

PMA P070022↗

FDA record

Trust

Unverified

Source FDA PMA, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA PMAAPPR Approved 1 supplement NumberP070022 Date9 Aug 2011ApprovedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA PMA Active

Specification

PMA

Generic name
Laparoscopic contraceptive tubal occlusion device
PMA number
FDA product code
KNH
Device class
Class III
Regulation
21 CFR Part 884.5380
Advisory committee
Obstetrics/Gynecology
FDA decision
APPR Approved
PMA supplement
S020

Overview

AI-generated summary, 18 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Adiana Permanent Contraception System is a laparoscopic contraceptive tubal occlusion device designed for permanent contraception. It functions by facilitating the occlusion of the fallopian tubes to prevent pregnancy.

This device is manufactured by Hologic, Inc. and is regulated under FDA PMA number P070022. It is classified as a class 3 medical device under regulation number 884.5380 for use in obstetrics and gynecology procedures.

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