Data / Medical devices / Honduras / E.M. Adams De Honduras
E.M. Adams De Honduras: FDA-registered device maker in CHOLOMA Cortes, Honduras, 1 510(k) clearance
E.M. Adams De Honduras is registered with the FDA (registration 3006089112) in CHOLOMA Cortes, Honduras. It lists 7 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 6, 1997. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3006089112
- Address
- Parque Inhdelva, Edificio 8F, CHOLOMA Cortes, Honduras, --
- Owner or operator
- E.M. ADAMS COMPANY (9003732)
- Roles
- Manufacturer
- First device listed
- May 13, 1997
- Registered through
- 2026
- Brand names listed
- ADAMS ABDOMINAL BINDER, ADAMS ORTHOSIS, ADAMS PROTECTIVE RESTRAINT, ADAMS SLING, ADAMS SPLINT, ADAMS SPLINT TRACTION, Body Holder, E.M. Adams Company and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Aid, Transfer | IKX | 1 | Manufacturer | accessdata.fda.gov |
| Binder, Abdominal | FSD | 1 | Manufacturer | accessdata.fda.gov |
| Orthosis, Limb Brace | IQI | 1 | Manufacturer | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Manufacturer | accessdata.fda.gov |
| Restraint, Protective | FMQ | 1 | Manufacturer | accessdata.fda.gov |
| Sling, Arm | ILI | 1 | Manufacturer | accessdata.fda.gov |
| Splint, Traction | HSP | 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 |
|---|---|---|---|---|---|---|
| August 6, 1997 | K971948 | PATIENT RESTRAINT | FMQ | Substantially Equivalent | E.M. Adams Co., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Protector, Skin Pressure
- All makers of Orthosis, Limb Brace
- All makers of Restraint, Protective
- All makers of Binder, Abdominal
- All makers of Aid, Transfer
- All makers of Splint, Traction
Updated August 6, 1997. 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.