Skip to the page
Get started – free

Data / Medical devices / Nerve Block Tray

Nerve Block Tray (OGJ): 17 FDA-registered makers in 4 countries

17 establishments in 4 countries are registered with the FDA to make Nerve Block Tray (product code OGJ, Class 2, 21 CFR 868.5140). 0 of them have a 510(k) clearance or PMA approval on file and 3 have a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 20 recall events (5 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.

Get every maker of this deviceMakers in the United StatesWatch this device
Product code
OGJ
Device class
2
Regulation
868.5140
Medical specialty
Anesthesiology

Makers by country

CountryMakers
United States14
Canada1
Mexico1
Honduras1

Makers of Nerve Block Tray

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
Argon Medical Devices Inc.Athens, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Avid Medical, Inc. A Medical Action Ind. Company 305Toano, VA, United StatesManufacturer, Repackager or relabeler0010api.fda.gov
B. Braun Medical Inc.Bethlehem, PA, United StatesSpecification developer0000api.fda.gov
B. Braun Us Device Manufacturing LLCAllentown, PA, United StatesContract manufacturer0000api.fda.gov
Busse Hospital DisposablesHauppauge, NY, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0020api.fda.gov
CHS USA IncorporatedPeachtree City, GA, United StatesSpecification developer0000api.fda.gov
Custom Interventional Pain ManagementSan Antonio, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Canadian Hospital Specialties Ltd.OAKVILLE Ontario, CanadaContract manufacturer0000api.fda.gov
Cardinal Health 200, LLCEl Paso, TX, United StatesManufacturer0000api.fda.gov
Convertors de Mexico S. de R.L. de C.VCD.JUAREZ Chihuahua, MexicoManufacturer0000api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Honduras Kitting, S.A.Villanueva Cortes, HondurasContract manufacturer0000api.fda.gov
Medical Action Industries, Inc. 306Arden, NC, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0022api.fda.gov
MEDLINE INDUSTRIES, LP - LaredoLaredo, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Medline Industries, LP - SPTWaukegan, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Vygon UsaLansdale, PA, United StatesSpecification developer0000api.fda.gov
Vygon MFGDover, NH, United StatesManufacturer0000api.fda.gov

Updated November 2, 2026. 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.