Safepath Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Safepath Medical, Inc. makes
Safepath Medical, Inc. manufactures silk sutures and suturing systems, including variations with polyamide (nylon) and polypropylene sutures. These products are designed for surgical applications requiring absorbable or non-absorbable thread materials.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and Unique Device Identifier (UDI) databases. The portfolio is regulated in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
SafePath Suturing System Ref K180701
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Company details
- DUNS number
- 877189584
Frequently asked questions
How many devices does Safepath Medical, Inc. have in the registry?
The registry currently lists 4 devices for Safepath Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Safepath Medical, Inc.'s devices?
Among its 4 most recently registered devices, Safepath Medical, Inc. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Safepath Medical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Safepath Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Safepath Medical, Inc. in the registry?
The most recently registered devices listed for Safepath Medical, Inc. include SafePath 1F001, SafePath 1F002, SafePath Suturing System and SafePath Sulturing System-Silk Suture, SafePath Sulturing System Polyamide Suture (Nylon) SafePath Sulturing System- Polypropylene Suture.