Covidien LP, Formerly Registered AS United States
United StatesFDA applicant, unverified
- Devices
- 8
What Covidien LP, Formerly Registered AS United States makes
The company manufactures single-use laparoscopic surgical instruments, including graspers, dissectors, shears, hooks, and suturing devices designed for minimally invasive procedures. Stapling systems with reusable staplers and single-use loading units are also part of the portfolio, alongside absorbable fixation devices and trocars for port placement. Tissue adhesives for surgical applications are included, as are modified endoscopic suturing tools.
These devices are classified as Class II under FDA regulations, with most authorised via 510(k) premarket notifications and some through PMA submissions. The products are listed in the FDA’s regulatory databases, and the company operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Sils Stitch Endoscopic Suturing Device Ref K090419
Regimes: 510(k) Registry: 510(k)Sils Port, Models SILSPT5, SILSPT12 Ref K082619
Regimes: 510(k) Registry: 510(k)Modified Endo Stich Ref K082659
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Indermil(Tm) Tissue Adhesive Ref P010002
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does Covidien Lp, Formerly Registered AS United States have in the registry?
The registry currently lists 8 devices for Covidien Lp, Formerly Registered AS United States. Devices recorded under merged duplicate company entries are counted once.
Which registries list Covidien Lp, Formerly Registered AS United States's devices?
Among its 8 most recently registered devices, Covidien Lp, Formerly Registered AS United States has devices listed in FDA 510(k) (7 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Covidien Lp, Formerly Registered AS United States's devices fall under?
Among its 8 most recently registered devices, the classes recorded for Covidien Lp, Formerly Registered AS United States's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Covidien Lp, Formerly Registered AS United States in the registry?
The most recently registered devices listed for Covidien Lp, Formerly Registered AS United States include SILS CLINCHER, SILS DISSECTOR, SILS GRASPER, SILS L-HOOK, SILS SHEARS, AUTOSUTURE ENDO GIA STAPLERS WITH ENDO GIA SINGLE USE LOADING UNITS, ABSORBATACK 5MM SINGLE USE ABSORBABLE FIXATION DEVICE and SILS STITCH ENDOSCOPIC SUTURING DEVICE.