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Midmark 153678WL

by Midmark Corporation

Midmark 153678WL is a Class I device made by Midmark Corporation, cleared under FDA 510(k) K003090 on 18 Oct 2000 and listed in FDA GUDID since 28 Sep 2026 (UDI-DI 00841709110054), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

510(k) K003090

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841709110054 UDI-DI Date28 Sep 2026ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Abbreviated NumberK003090 Date18 Oct 2000DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K003090 decided 18 Oct 2000 Active
  • FDA GUDID UDI-DI 00841709110054 listed 28 Sep 2026 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K003090
  2. Listed FDA GUDID 00841709110054

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Midmark
Generic name
Dental delivery system instrument unit, electric
Model / Ref / Catalog
153678WL
Primary DI / UDI-DI
00841709110054
510(k) Number
FDA product code
EIA
GMDN term
Dental delivery system instrument unit, electric
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K003090)

and 8 more cleared under K003090

Similar devices

Other devices filed under FDA product code EIA (Unit, operative dental).

Other devices from Midmark Corporation

See all devices from Midmark Corporation →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)