Data / Medical devices / Ring (Wound Protector), Drape Retention, Internal / United States
FDA-registered makers of Ring (Wound Protector), Drape Retention, Internal in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Ring (Wound Protector), Drape Retention, Internal (product code KGW). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Ring (Wound Protector), Drape Retention, Internal
- Product code
- KGW
- Country
- United States
Makers of Ring (Wound Protector), Drape Retention, Internal in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Applied Medical Resources Corp. | Rsm, CA, United States | Complaint file establishment, Manufacturer | 3 | April 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Applied Medical Distribution Center | Irvine, CA, United States | Manufacturer | 3 | April 24, 2026 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Isomedix Operations Inc. | Whippany, NJ, United States | Contract sterilizer, Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum Us LLC | Eagan, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surgentec LLC | Boca Raton, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum US LLC | San Antonio, TX, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Solventum US LLC | Brookings, SD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| VLV Associates, Inc. | Whippany, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. 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.