Data / Medical devices / United States / E.M. Adams Co., Inc.
E.M. Adams Co., Inc.: FDA-registered device maker in Fort Pierce, FL, United States, 3 510(k) clearances
E.M. Adams Co., Inc. is registered with the FDA (registration 1054786) in Fort Pierce, FL, United States. It lists 6 device types. The FDA files 3 510(k) clearances 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
- 1054786
- FEI number
- 1000114163
- Address
- 7496 Commercial Circle, Fort Pierce, FL, United States, 34951
- Owner or operator
- E.M. ADAMS COMPANY (9003732)
- Roles
- Manufacturer
- First device listed
- May 13, 1997
- Registered through
- 2026
- Brand names listed
- ADAMS PROTECTIVE RESTRAINT, Body Holder, E.M. Adams Company, Elbow Splint, Knee Brace, Knee Splint, Limb Holder, Mitt and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Aid, Transfer | IKX | 1 | Manufacturer | accessdata.fda.gov |
| Joint, Knee, External Brace | ITQ | 1 | Manufacturer | accessdata.fda.gov |
| Protector, Skin Pressure | FMP | 1 | Manufacturer | accessdata.fda.gov |
| Restraint, Protective | FMQ | 1 | Manufacturer | accessdata.fda.gov |
| Suture Removal Kit | MCZ | 1 | Manufacturer | accessdata.fda.gov |
| Tray, Surgical, Instrument | FSM | 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 |
| January 8, 1982 | K812133 | WOUND CLOSURE INSTRUMENT TRAY | FSM | Substantially Equivalent | E.M. Adams | accessdata.fda.gov |
| December 1, 1981 | K812132 | STERILE SUTURE REMOVAL KIT | MCZ | Substantially Equivalent | E.M. Adams | accessdata.fda.gov |
Compare with other makers
- All makers of Aid, Transfer
- All makers of Protector, Skin Pressure
- All makers of Tray, Surgical, Instrument
- All makers of Restraint, Protective
- All makers of Joint, Knee, External Brace
- All makers of Suture Removal Kit
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.