DeviceClearance

Product code JDR— Orthopedic

COMPRESSYN STAPLE

Classification name
Staple, Fixation, Bone
Device class
Class 2
Regulation
21 CFR 888.3030
Advisory panel
Orthopedic
Total cleared
232
First cleared
Most recent

Market context for product code JDR

FDA has cleared 232 devices under product code JDR between 1979 and 2026, filed by 124 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 JDR

Adverse events under product code JDR

product code JDR
Injury
726
Malfunction
663
Other
1
Total
1,390

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 JDR

1–100 of 232

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