Data / Medical devices / Jordan
Medical device makers in Jordan: 2 FDA-registered establishments
2 establishments in Jordan are registered with the FDA to make medical devices for the US market, listing 19 device types. 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- JordanCountry
Device types made here
Device types with the most registered makers in this country.
| Device | Product code | Makers |
|---|---|---|
| Enzyme Immunoassay, Cocaine And Cocaine Metabolites | DIO | 1 |
| Enzyme Immunoassay, Cannabinoids | LDJ | 1 |
| Enzyme Immunoassay, Opiates | DJG | 1 |
| Enzyme Immunoassay, Propoxyphene | JXN | 1 |
| Enzyme Immunoassay, Benzodiazepine | JXM | 1 |
| Enzyme Immunoassay, Amphetamine | DKZ | 1 |
| Enzyme Immunoassay, Methadone | DJR | 1 |
| Enzyme Immunoassay, Phencyclidine | LCM | 1 |
| Enzyme Immunoassay, Barbiturate | DIS | 1 |
| Nitroprusside, Ketones (Urinary, Non-Quant.) | JIN | 1 |
| Azo-Dyes, Colorimetric, Bilirubin & Its Conjugates (Urinary, Non-Quant.) | JJB | 1 |
| Indicator Method, Protein Or Albumin (Urinary, Non-Quant.) | JIR | 1 |
| Test, Urine Leukocyte | LJX | 1 |
| Radioimmunoassay, Tricyclic Antidepressant Drugs | LFG | 1 |
| Thin Layer Chromatography, Methamphetamine | DJC | 1 |
| Test, Luteinizing Hormone (Lh), Over The Counter | NGE | 1 |
| Kit, Test, Pregnancy, Hcg, Over The Counter | LCX | 1 |
| Thin Layer Chromatography, Morphine | DNK | 1 |
| Aligner, Sequential | NXC | 1 |
Makers in Jordan
Best documented first: most 510(k) clearances and PMA approvals.
| Maker | Location | Device types | 510(k) clearances | PMA approvals | Recall events | Source |
|---|---|---|---|---|---|---|
| Atlas Medical | Amman Al 'Asimah, Jordan | 18 | 2 | 0 | 0 | api.fda.gov |
| Eon Dental Jordan (Free Zones) | Amman Al 'Asimah, Jordan | 1 | 1 | 0 | 0 | api.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.