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iScreen™ ABTDUAW17703C

by Instant Technologies, Inc.

iScreen ABTDUAW17703C is a multiple drugs of abuse IVD (FDA Class II) made by Instant Technologies, Inc., cleared under FDA 510(k) K182701 on 3 Dec 2018 and listed in FDA GUDID since 9 Nov 2022 (UDI-DI 00817405023424), active as of 22 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

1 ongoing

Recall on shared 510(k) K182701; other models may be affected

Documents

510(k) K182701

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817405023424 UDI-DI Date9 Nov 2022ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK182701 Date3 Dec 2018DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K182701 decided 3 Dec 2018 Active
  • FDA GUDID UDI-DI 00817405023424 listed 9 Nov 2022 Listed

Recalls

1 recall · 1 ongoing · FDA

    • Ongoing Z-1589-2022 FDA Class II initiated 25 May 2022 on shared 510(k) K182701

    Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.

Recalls on a shared submission name another device cleared under the same FDA submission as this one.

Timeline

3 dated events

  1. Cleared FDA 510(k) K182701
  2. Recall initiated FDA recalls Z-1589-2022
  3. Listed FDA GUDID 00817405023424

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
iScreen™
Generic name
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Model / Ref / Catalog
ABTDUAW17703C
Description
7 PANEL CLIA WAIVED ROUND CUP AMP1000, COC300, MET500, MOP300, OXY100, PCP25, THC50 SVT (CR, NI, OX, pH, S.G.)
Primary DI / UDI-DI
00817405023424
510(k) Number
FDA product code
NFT, NFY, NGG, NGL, LCM, NFW
GMDN term
Multiple drugs of abuse IVD, kit, rapid ICT, clinical
Device class
Class II
Regulation number
862.3100, 862.3250, 862.3610, 862.3650, 862.3870
GUDID distribution status
In Commercial Distribution

Related devices

Category: Multiple drugs of abuse IVD, kit, rapid ICT, clinical

Cleared under the same submission (K182701)

and 8 more cleared under K182701

Similar devices

Other devices filed under FDA product code NFT (Test, Amphetamine, Over The Counter).

Other devices from Instant Technologies, Inc.

See all devices from Instant Technologies, Inc. →

Properties

  • Single use
  • Prescription use
  • Over-the-counter
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)