Interlace Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Myosure Rod Lens Scope Seals Ref K102686
Regimes: 510(k) Registry: 510(k)Surgisure Tissue Removal System Ref K103741
Regimes: 510(k) Registry: 510(k)Myosure Rod Lens Hysteroscope Ref K091465
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Myosure Hysteroscopic Tissue Removal System Ref K091100
Regimes: 510(k) Registry: 510(k)Interlace Medical Operative Hysteroscopy System Ref K081070
Regimes: 510(k) Registry: 510(k)Myosure Hysteroscopic Tissue Removal System Ref K100559
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Interlace Medical, Inc. have in the registry?
The registry currently lists 7 devices for Interlace Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interlace Medical, Inc.'s devices?
Among its 7 most recently registered devices, Interlace Medical, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Interlace Medical, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Interlace Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Interlace Medical, Inc. in the registry?
The most recently registered devices listed for Interlace Medical, Inc. include MYOSURE ROD LENS SCOPE SEALS, SURGISURE TISSUE REMOVAL SYSTEM, MYOSURE ROD LENS HYSTEROSCOPE and INTERLACE MEDICAL HYSTEROSCOPIC MORCELLATION SYSTEM.