Data / Medical devices / United States / Med Way Inc.
Med Way Inc.: FDA-registered device maker in Buford, GA, United States, 1 510(k) clearance
Med Way Inc. is registered with the FDA (registration 3012084379) in Buford, GA, United States. It lists 10 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 19, 2024. Registered through 2026. FDA data exported November 3, 2026.
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- FDA registration number
- 3012084379
- Address
- 1650 Horizon PKWY NE, Suite 450, Buford, GA, United States, 30518
- Owner or operator
- Med Way Inc. (10050401)
- Roles
- Manufacturer
- First device listed
- May 4, 2020
- Registered through
- 2026
- Brand names listed
- Adhesive Tape and Bandage; Silicone Tape, Alginate Dressing; Acne Patch, Film Dressing, Hydrocolloid Dressing; Hydrocolloid Foam Dressing; Foam Dressing Kit, Hydrogel Dressing, Negative Pressure Wound Therapy Device, V-Move, V-Grand, Nonwoven Island Dressing/Sponge; Nonresorbable for External Use, Scar Gel Sheet and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Intravascular Catheter Securement | KMK | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Hydrogel Without Drug And/Or Biologic | NAE | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Hydrophilic | NAC | 1 | Manufacturer | accessdata.fda.gov |
| Dressing, Wound, Occlusive | NAD | 1 | Manufacturer | accessdata.fda.gov |
| Elastomer, Silicone, For Scar Management | MDA | 1 | Manufacturer | accessdata.fda.gov |
| Gauze / Sponge,Nonresorbable For External Use | NAB | 1 | Manufacturer | accessdata.fda.gov |
| Mattress, Air Flotation, Alternating Pressure | FNM | 2 | Manufacturer | accessdata.fda.gov |
| Negative Pressure Wound Therapy Powered Suction Pump | OMP | 2 | Manufacturer | accessdata.fda.gov |
| Silicone Hydrogel For Scar Management | PFP | 1 | Manufacturer | accessdata.fda.gov |
| Tape And Bandage, Adhesive | KGX | 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 19, 2024 | K241023 | Negative Pressure Wound Therapy Device (V-Move, V-Grand) | OMP | Substantially Equivalent | Med Way, Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of Device, Intravascular Catheter Securement
- All makers of Gauze / Sponge,Nonresorbable For External Use
- All makers of Tape And Bandage, Adhesive
- All makers of Negative Pressure Wound Therapy Powered Suction Pump
- All makers of Elastomer, Silicone, For Scar Management
- All makers of Dressing, Wound, Hydrophilic
Updated August 19, 2024. 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.