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Manuka Fill

by Links Medical Products, Inc.

510(k) K121227

Manuka Fill is a device classified as Unclassified made by Links Medical Products, Inc., cleared under FDA 510(k) K121227 on 23 May 2012, active as of 23 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK121227 Date23 May 2012ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
FRO
Device class
U
Advisory committee
Unknown
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code FRO (Dressing, Wound, Drug).

Other devices from Links Medical Products, Inc.

  • LMP Manuka IG WC20

    Unclassified
  • LMP Manuka Fill WC07 Open recall

    Unclassified
  • LinkTemp LMP001

    Class II
  • LMP Manuka IG Max WC25

    Unclassified

See all devices from Links Medical Products, Inc. →