Data / Medical devices / Drape, Patient, Ophthalmic / United States
FDA-registered makers of Drape, Patient, Ophthalmic in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Drape, Patient, Ophthalmic (product code HMT). 3 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Drape, Patient, Ophthalmic
- Product code
- HMT
- Country
- United States
Makers of Drape, Patient, Ophthalmic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Atlanta Healthcare Services | Lawrenceville, GA, United States | Repackager or relabeler, Specification developer | 1 | February 13, 1986 | 0 | 0 | 0 | api.fda.gov |
| Alcon Research, LLC | Fort Worth, TX, United States | Specification developer | 1 | April 6, 1983 | 0 | 1 | 0 | api.fda.gov |
| Alcon Research, LLC | Houston, TX, United States | Manufacturer | 1 | April 6, 1983 | 0 | 0 | 0 | api.fda.gov |
| Cardinal Health | Hazelwood, MO, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Foothills Industries, Inc. | Marion, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Haywood Vocational Opportunities Inc. | Waynesville, NC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Imentum Medical LLC | Irvine, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marble Medical, Inc. | Tallahassee, FL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microtek Medical LLC | Eagan, MN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microtek Medical LLC | Alpharetta, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weslacova | North Wilkesboro, NC, United States | Contract 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.