DeviceClearance

Product code JOS— General, Plastic Surgery

BIPOLAR FORCEPS

Classification name
Electrode, Electrosurgical
Device class
Class 2
Regulation
21 CFR 878.4400
Advisory panel
General, Plastic Surgery
Total cleared
36
First cleared
Most recent

Market context for product code JOS

FDA has cleared 36 devices under product code JOS between 1977 and 2016, filed by 27 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code JOS

Recent clearances under product code JOS

Data sourced from openFDA. This site is unofficial and independent of the FDA.