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MeCare Alpha (MCA2019)

by IVT Medical, Ltd.

510(k) K260426

MeCare Alpha (MCA2019) is a Class II device made by IVT Medical, Ltd., cleared under FDA 510(k) K260426 on 8 Oct 2026, active as of 8 Nov 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 8 Nov 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK260426 Date8 Oct 2026ClearedStatusActive

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  • Withdrawn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
OMP
Device class
Class II
Regulation
21 CFR Part 878.4780
Advisory committee
General, Plastic Surgery
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code OMP (Negative Pressure Wound Therapy Powered Suction Pump).

Other devices from IVT Medical, Ltd.

  • Vcare a

    Class II