DeviceClearance

Product code FZP— General, Plastic Surgery

IMPLANTABLE CLIP

Classification name
Clip, Implantable
Device class
Class 2
Regulation
21 CFR 878.4300
Advisory panel
General, Plastic Surgery
Total cleared
177
First cleared
Most recent

Market context for product code FZP

FDA has cleared 177 devices under product code FZP between 1977 and 2026, filed by 82 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 FZP

Adverse events under product code FZP

product code FZP
Death
11
Injury
726
Malfunction
10,830
Other
1
Total
11,568

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 FZP

1–100 of 177

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