S4 Medical Corp.
United StatesFDA 510(k) applicant, unverified
- Devices
- 7
What S4 Medical Corp. makes
S4 Medical Corp. manufactures the esolution, a surgical retractor designed for esophageal procedures, and the esolution® Esophageal Retractor, a specialized tool for minimally invasive surgeries in the esophageal region.
The company’s products fall under FDA Class II devices and are listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
- GUDID
- GUDID
- GUDID
- GUDID
- GUDID
esolution Ref DEN230006
De Novo 510(k)esolution® Esophageal Retractor Ref K243233
510(k) 510(k)
Company details
- DUNS number
- 081128564
Frequently asked questions
How many devices does S4 Medical Corp. have in the registry?
The registry currently lists 7 devices for S4 Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list S4 Medical Corp.'s devices?
Among its 7 most recently registered devices, S4 Medical Corp. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (5 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do S4 Medical Corp.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for S4 Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from S4 Medical Corp. in the registry?
The most recently registered devices listed for S4 Medical Corp. include esolution Esophageal Retractor OPS 30-0005, esolution Esophageal Retractor OPS-temp 30-0004, esolution Esophageal Retractor 30-0001 and esolution Esophageal Retractor PRECISION - temp 30-0002.