Aragon Surgical, Inc.
United StatesFDA applicant, unverified
- Devices
- 6
What Aragon Surgical, Inc. makes
Aragon Surgical, Inc. manufactures radiofrequency (RF) ablation instruments and laparoscopic devices, including the ARAGON ONESHOT SYSTEM for tissue ablation, the ARAGON SURGICAL LAPCAP for laparoscopic applications, and various RF system instruments (e.g., TELEO, L2, and 5mm laparoscopic probes) designed for surgical energy delivery.
The company’s portfolio is classified under FDA’s Class II regulatory category and is authorised via 510(k) clearance. These devices are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
Aragon Oneshot System Ref K081312
Regimes: 510(k) Registry: 510(k)Aragon Surgical Lapcap Ref K070651
Regimes: 510(k) Registry: 510(k)Aragon Surgical Rf System Teleo Instrument Ref K093075
Regimes: 510(k) Registry: 510(k)Modification To: Aragon Surgical Lapcap Ref K073452
Regimes: 510(k) Registry: 510(k)Aragon Surgical Rf System L2 Instrument Ref K090306
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aragon Surgical, Inc. have in the registry?
The registry currently lists 6 devices for Aragon Surgical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aragon Surgical, Inc.'s devices?
Among its 6 most recently registered devices, Aragon Surgical, Inc. has devices listed in FDA 510(k) (6 devices).
What risk classes do Aragon Surgical, Inc.'s devices fall under?
Among its 6 most recently registered devices, the classes recorded for Aragon Surgical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aragon Surgical, Inc. in the registry?
The most recently registered devices listed for Aragon Surgical, Inc. include ARAGON ONESHOT SYSTEM, ARAGON SURGICAL LAPCAP, ARAGON SURGICAL RF SYSTEM TELEO INSTRUMENT and MODIFICATION TO: ARAGON SURGICAL LAPCAP.