Teleflex Medical Incorporated
United StatesFDA applicant, unverified
- Devices
- 3
What Teleflex Medical Incorporated makes
Teleflex Medical Incorporated manufactures absorbable and non-absorbable sutures, including monofilament and braided variants, designed for soft tissue and orthopedic applications. Their product line includes sutures like Force Fiber, Bondek, Monodek, and Polyglytone*6211, as well as specialized tapes and fusion sutures for surgical use.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company’s products are listed in the FDA’s 510(k) database, reflecting their regulatory authorization in the United States.
Catalogue
Force Fiber Suture Ref K191268
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Force Fiber Fusion Suture Ref K172016
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Teleflex Medical Incorporated have in the registry?
The registry currently lists 3 devices for Teleflex Medical Incorporated. Devices recorded under merged duplicate company entries are counted once.
Which registries list Teleflex Medical Incorporated's devices?
Among its 3 most recently registered devices, Teleflex Medical Incorporated has devices listed in FDA 510(k) (3 devices).
What risk classes do Teleflex Medical Incorporated's devices fall under?
Among its 3 most recently registered devices, the classes recorded for Teleflex Medical Incorporated's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Teleflex Medical Incorporated in the registry?
The most recently registered devices listed for Teleflex Medical Incorporated include Force Fiber Suture, Force Fiber White and White/Blue, White/Black, Blue, and White/Green sutures; Force Fiber OrthoTape suture; Bondek suture and Bondek Plus suture; Monodek suture; Polyglytone*6211 suture and Force Fiber Fusion Suture.