Skip to the page

Data / Medical devices / Igg, Fitc, Antigen, Antiserum, Control

Igg, Fitc, Antigen, Antiserum, Control (DGK): 3 FDA-registered makers in 3 countries

3 establishments in 3 countries are registered with the FDA to make Igg, Fitc, Antigen, Antiserum, Control (product code DGK, Class 2, 21 CFR 866.5510). 2 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 2 510(k) clearances under this code, the latest on July 18, 1983, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

Product code
DGK
Device class
2
Regulation
866.5510
Medical specialty
Immunology

Makers by country

CountryMakers
Denmark1
Singapore1
United States1

Makers of Igg, Fitc, Antigen, Antiserum, Control

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Agilent Technologies Denmark ApSGLOSTRUP Hovedstaden, DenmarkManufacturer1July 18, 1983000api.fda.gov
Agilent Technologies Singapore (International) Pte Ltd.Singapore North East, SingaporeSpecification developer1July 18, 1983000api.fda.gov
Kent Laboratories, Inc.Bellingham, WA, United StatesManufacturer0000api.fda.gov

Updated July 18, 1983. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.