DeviceClearance

Product code JDQ— Orthopedic

COMPRESSYN BAND

Classification name
Cerclage, Fixation
Device class
Class 2
Regulation
21 CFR 888.3010
Advisory panel
Orthopedic
Total cleared
130
First cleared
Most recent

Market context for product code JDQ

FDA has cleared 130 devices under product code JDQ between 1984 and 2026, filed by 73 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 JDQ

Adverse events under product code JDQ

product code JDQ
Death
9
Injury
330
Total
339

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code JDQ

1–100 of 130

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