Adam Spencer Corp.
United StatesFDA applicant, unverified
- Devices
- 5
What Adam Spencer Corp. makes
Adam Spencer Corp. manufactures angiographic catheters, including the MAXI-TORQUE PLUS SOFTIP model, designed for vascular imaging procedures. Their portfolio also includes high-pressure braided tubes, such as the ASC series, intended for specialized medical applications requiring reinforced tubing.
These devices are classified under Class II by the FDA and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Maxi-Torque Plus Softip Angiographic Catheter Ref K963092
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Maxi-Torque Plus Angiographic Catheter Ref K955111
Regimes: 510(k) Registry: 510(k)Asc High Pressure Braided Tubes Ref K964331
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adam Spencer Corp. have in the registry?
The registry currently lists 5 devices for Adam Spencer Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adam Spencer Corp.'s devices?
Among its 5 most recently registered devices, Adam Spencer Corp. has devices listed in FDA 510(k) (5 devices).
What risk classes do Adam Spencer Corp.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Adam Spencer Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adam Spencer Corp. in the registry?
The most recently registered devices listed for Adam Spencer Corp. include EZ-INTRO PERCUTANEOUS CATHETER SHEATH, EZ-INTRO VESSEL DILATOR, MAXI-TORQUE PLUS SOFTIP ANGIOGRAPHIC CATHETER, ASE MAXI-TORQUE, SUPPLE FLEX ANGIOGRAPHIC CATHETERS and MAXI-TORQUE PLUS ANGIOGRAPHIC CATHETER.