Rocket of London, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 3
What Rocket of London, Ltd. makes
Rocket of London, Ltd. manufactures surgical instruments, including suture-removing forceps for wound closure, intrauterine sound devices for gynecological measurements, and the Uriglow transilluminating ureteric stent for diagnostic visualization of urinary obstructions.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. Their portfolio is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Suture Removing Forceps Ref K932385
Regimes: 510(k) Registry: 510(k)Intrauterine Sound Ref K935665
Regimes: 510(k) Registry: 510(k)Uriglow Transilluminating Ureteric Stent Model Ref K943801
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rocket of London, Ltd. have in the registry?
The registry currently lists 3 devices for Rocket of London, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rocket of London, Ltd.'s devices?
Among its 3 most recently registered devices, Rocket of London, Ltd. has devices listed in FDA 510(k) (3 devices).
What risk classes do Rocket of London, Ltd.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Rocket of London, Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Rocket of London, Ltd. in the registry?
The most recently registered devices listed for Rocket of London, Ltd. include SUTURE REMOVING FORCEPS, INTRAUTERINE SOUND and URIGLOW TRANSILLUMINATING URETERIC STENT MODEL.