Data / Medical devices / United States / Sweat Institute
Sweat Institute: FDA-registered device maker in Atlanta, GA, United States, 1 510(k) clearance
Sweat Institute is registered with the FDA (registration 1039671) in Atlanta, GA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 21, 1995. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1039671
- Address
- 3312 Chamblee Tucker Rd, Atlanta, GA, United States, 30341
- Owner or operator
- SWEAT INSTITUTE FOR ATLAS ORTHOGONAL (1039671)
- Roles
- Manufacturer
- First device listed
- April 24, 2024
- Registered through
- 2026
- Brand names listed
- Atlas Orthogoanl Instrument
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Manipulator, Plunger-Like Joint | LXM | U | 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 |
|---|---|---|---|---|---|---|
| November 21, 1995 | K951217 | ATLAS ORTHOGONAL PERCUSSION INSTTUMENT | LXM | Substantially Equivalent | Sweat Chiropractic Clinic | accessdata.fda.gov |
Compare with other makers
Updated November 21, 1995. 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.