Skip to content

Trinity Biotech 32-5010

by Mardx Diagnostics, Inc.

Trinity Biotech 32-5010 is a Class II device made by Mardx Diagnostics, Inc., cleared under FDA 510(k) K890053 on 18 Apr 1989 and listed in FDA GUDID since 18 Sep 2016 (UDI-DI 05391516747608), 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) K890053

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 Number05391516747608 UDI-DI Date18 Sep 2016ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK890053 Date18 Apr 1989DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K890053 decided 18 Apr 1989 Active
  • FDA GUDID UDI-DI 05391516747608 listed 18 Sep 2016 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K890053
  2. Listed FDA GUDID 05391516747608

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Trinity Biotech
Generic name
Borrelia burgdorferi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Model / Ref / Catalog
32-5010
Description
B. burgdorferi 10 Well Slides, 10 each pack
Primary DI / UDI-DI
05391516747608
510(k) Number
FDA product code
LSR
GMDN term
Borrelia burgdorferi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Device class
Class II
Regulation number
866.3830
GUDID distribution status
In Commercial Distribution

Related devices

Category: Borrelia burgdorferi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Cleared under the same submission (K890053)

Similar devices

Other devices filed under FDA product code LSR (Reagent, Borrelia Serological Reagent).

Other devices from Mardx Diagnostics, Inc.

See all devices from Mardx Diagnostics, Inc. →

Properties

  • Single use
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)