DeviceClearance

Product code HQB— Ophthalmic

23GA CURVED ILLUMINATING LASER PROBE

Classification name
Photocoagulator And Accessories
Device class
Class 2
Regulation
21 CFR 886.4690
Advisory panel
Ophthalmic
Total cleared
30
First cleared
Most recent

Market context for product code HQB

FDA has cleared 30 devices under product code HQB between 1976 and 2022, filed by 20 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 HQB

Adverse events under product code HQB

product code HQB
Other
2
Total
2

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 HQB

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