Data / Medical devices / United States / Medline Industries, LP - Lithia Springs
Medline Industries, LP - Lithia Springs: FDA-registered device maker in Lithia Springs, GA, United States, 1 510(k) clearance
Medline Industries, LP - Lithia Springs is registered with the FDA (registration 1000110779) in Lithia Springs, GA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 24, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1000110779
- Address
- 9103 Riverside Pkwy, Lithia Springs, GA, United States, 30122
- Owner or operator
- Medline Industries, LP (1417592)
- Roles
- Manufacturer
- First device listed
- January 1, 1992
- Registered through
- 2026
- Brand names listed
- BEDDING, CleanOp: bedding and cleaning supplies, ComfortGlide Drypad, DISPOSABLE BEDDING, Extrasorb, FitRight, FitRight ActivEdge Bladder Control Pads, FitRight ActivEdge Male Guard and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Bedding, Disposable, Medical | KME | 1 | Manufacturer | accessdata.fda.gov |
| Garment, Protective, For Incontinence | EYQ | 1 | Manufacturer | accessdata.fda.gov |
| Mask, Surgical | FXX | 2 | 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 |
|---|---|---|---|---|---|---|
| March 24, 2023 | K223236 | Medline Surgical Face Mask and Medline Procedural Face Mask | FXX | Substantially Equivalent | Medline Industries, LP | accessdata.fda.gov |
Compare with other makers
- All makers of Garment, Protective, For Incontinence
- All makers of Mask, Surgical
- All makers of Bedding, Disposable, Medical
Updated March 24, 2023. 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.