Endolap, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What Endolap, Inc. makes
Endolap, Inc. manufactures medical devices including the ENDOLAP RESECTOSCOPE CUTTING LOOP ELECTRODE, TITAN INSUFFLATION NEEDLE, ESYS SYSTEM, ENDOLAP INSUFFLATOR TUBING SET, and ENDOLAP RESECTOSCOPE ROLLER ELECTRODE.
The company's devices are all Class II and listed in the FDA 510(k) registry. Endolap, Inc. is based in the US.
Catalogue
Endolap Resectoscope Cutting Loop Electrode Ref K974516
Regimes: 510(k) Registry: 510(k)Titan Insufflation Needle Ref K950243
Regimes: 510(k) Registry: 510(k)Esys System Ref K933492
Regimes: 510(k) Registry: 510(k)Endolap Insufflator Tubing Set Ref K950219
Regimes: 510(k) Registry: 510(k)Endolap Resectoscope Roller Electrode Ref K974515
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endolap, Inc. have in the registry?
The registry currently lists 5 devices for Endolap, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endolap, Inc.'s devices?
Among its 5 most recently registered devices, Endolap, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Endolap, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Endolap, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endolap, Inc. in the registry?
The most recently registered devices listed for Endolap, Inc. include ENDOLAP RESECTOSCOPE CUTTING LOOP ELECTRODE, TITAN INSUFFLATION NEEDLE, ESYS SYSTEM and ENDOLAP INSUFFLATOR TUBING SET.