Data / Medical devices / United States / MJM International Corporation
MJM International Corporation: FDA-registered device maker in Edinburg, TX, United States, 1 510(k) clearance
MJM International Corporation is registered with the FDA (registration 3004499949) in Edinburg, TX, United States. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated December 5, 2005. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3004499949
- Address
- 801 E. Cano Street, Edinburg, TX, United States, 78539
- Owner or operator
- MJM INTERNATIONAL CORPORATION (9079487)
- Roles
- Manufacturer
- First device listed
- November 10, 2005
- Registered through
- 2027
- Brand names listed
- MULTIPLE POSITIONAL GERRY CHAIRS, SELF PROPELLED AQUATIC CHAIR, SERIES 400 WALKER, SHOWER CHAIRS, TINT-N-SPACE SLIDER, VARIOUS MODELS OF CRASH CARTS, VARIOUS MODELS OF LOW BEDS, VARIOUS MODELS OF SHOWER GURNEYS and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bars, Parallel, Exercise | IOE | 1 | Manufacturer | accessdata.fda.gov |
| Bed, Manual | FNJ | 1 | Manufacturer | accessdata.fda.gov |
| Cart, Emergency, Cardiopulmonary (Excluding Equipment) | BZN | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Adjustable, Mechanical | INN | 1 | Manufacturer | accessdata.fda.gov |
| Chair, Geriatric | FRJ | 1 | Manufacturer | accessdata.fda.gov |
| Chair, With Casters | INM | 1 | Manufacturer | accessdata.fda.gov |
| Device, Anti-Tip, Wheelchair | IMR | 1 | Manufacturer | accessdata.fda.gov |
| Device, Transfer, Patient, Manual | FMR | 1 | Manufacturer | accessdata.fda.gov |
| Stretcher, Wheeled | FPO | 2 | Manufacturer | accessdata.fda.gov |
| Walker, Mechanical, Poly Vinyl Chloride (Pvc) | NXE | 1 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 5, 2005 | K053192 | MODEL 418 SERIES WALKERS | NXE | Substantially Equivalent | Mjm International Corporation | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Transfer, Patient, Manual
- All makers of Walker, Mechanical, Poly Vinyl Chloride (Pvc)
- All makers of Chair, Geriatric
- All makers of Bars, Parallel, Exercise
- All makers of Device, Anti-Tip, Wheelchair
- All makers of Stretcher, Wheeled
Updated December 5, 2005. 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.