Glycar, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Glycar, Inc. makes
Glycar, Inc. manufactures medical devices including staple strips, tissue repair patches, pericardial patches, and uro-slings, which are part of their tissue repair patch family of products and vascular repair patch alternatives.
The company's devices are classified as Class II and listed in the FDA 510(k) registry. Glycar, Inc. is based in the US.
Catalogue
Glycar Staple Strips Ref K954665
Regimes: 510(k) Registry: 510(k)Glycar Tissue Repair Patch Ref K942911
Regimes: 510(k) Registry: 510(k)Glycar Pericardial Patch Ref K963967
Regimes: 510(k) Registry: 510(k)Glycar Tissue Repair Patch, Bio-Patch, Uro-Sling Ref K963175
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Glycar, Inc. have in the registry?
The registry currently lists 5 devices for Glycar, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Glycar, Inc.'s devices?
Among its 5 most recently registered devices, Glycar, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Glycar, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Glycar, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Glycar, Inc. in the registry?
The most recently registered devices listed for Glycar, Inc. include GLYCAR STAPLE STRIPS, GLYCAR TISSUE REPAIR PATCH, GLYCAR PERICARDIAL PATCH and GLYCAR TISSUE REPAIR PATCH, BIO-PATCH, URO-SLING.