Data / Medical devices / United States / Visionary Medical Supplies, Inc.

Visionary Medical Supplies, Inc.: FDA-registered device maker in Madison, WI, United States, 4 510(k) clearances

Name: Visionary Medical Supplies, Inc. FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Visionary Medical Supplies, Inc. is registered with the FDA (registration 1064514) in Madison, WI, United States. It lists 11 device types. The FDA files 4 510(k) clearances under its listings, the newest dated February 3, 2011. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 1064514
FEI number: 3004161528
Address: 6441 Enterprise Ln Ste 204, Madison, WI, United States, 53719
Owner or operator: VISIONARY MEDICAL SUPPLIES, INC. (9040860)
Roles: Manufacturer, Manufacturer for export, Specification developer
First device listed: August 12, 2004
Registered through: 2026
Brand names listed: SUTRALENE, SUTRALON, SUTRASILK, Sutrabond, Sutrazorb, VisiCoat, VisiCoat Plus, VisiCut and more

Devices it lists

Device	Product code	Class	Role	Source
Aid, Surgical, Viscoelastic	LZP	3	Manufacturer for export, Specification developer	accessdata.fda.gov
Fluid, Intraocular	LWL	3	Manufacturer for export, Specification developer	accessdata.fda.gov
Injector, Capsular Tension Ring	NCE	1	Manufacturer for export, Specification developer	accessdata.fda.gov
Intraocular Lens	HQL	3	Manufacturer for export, Specification developer	accessdata.fda.gov
Knife, Ophthalmic	HNN	1	Manufacturer	accessdata.fda.gov
Suture, Absorbable, Synthetic, Polyglycolic Acid	GAM	2	Manufacturer	accessdata.fda.gov
Suture, Nonabsorbable, Silk	GAP	2	Manufacturer	accessdata.fda.gov
Suture, Nonabsorbable, Synthetic, Polyamide	GAR	2	Manufacturer	accessdata.fda.gov
Suture, Nonabsorbable, Synthetic, Polyester	GAS	2	Manufacturer for export	accessdata.fda.gov
Suture, Nonabsorbable, Synthetic, Polypropylene	GAW	2	Manufacturer	accessdata.fda.gov
Trypan Blue	LGY	1	Specification developer	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
February 3, 2011	K102592	SUTRAZORB	GAM	Substantially Equivalent	Visionary Medical Supplies, Inc.	accessdata.fda.gov
April 17, 2007	K070243	SUTRALENE POLYPROPYLENE SUTURES	GAW	Substantially Equivalent	Visionary Medical Supplies, Inc.	accessdata.fda.gov
February 8, 2000	K994177	SUTRASILK SILK SUTURE	GAP	Substantially Equivalent	Visionary Medical Supplies, Inc.	accessdata.fda.gov
February 8, 2000	K994176	SUTRALON NYLON SUTURES	GAR	Substantially Equivalent	Visionary Medical Supplies, Inc.	accessdata.fda.gov

Compare with other makers

Updated February 3, 2011. 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.