Skip to content

Suture Removal Kit

by Medical Action Industries Inc.

510(k) K810685

Suture Removal Kit is a Class I device made by Medical Action Industries Inc., cleared under FDA 510(k) K810685 on 26 Mar 1981, active as of 22 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 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK810685 Date26 Mar 1981ClearedStatusActive

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  • Withdrawn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
GEN
FDA applicant
Medical Action Industries, Inc.
Device class
Class I
Regulation
21 CFR Part 878.4800
Advisory committee
General, Plastic Surgery
FDA decision
SESE Substantially Equivalent

Similar devices

Other devices filed under FDA product code GEN (Forceps, General & Plastic Surgery).

Other devices from Medical Action Industries Inc.

See all devices from Medical Action Industries Inc. →