DeviceClearance

Product code OKS— Unknown

ATRION MEDICAL COATED LACRIMAL INTUBATION SET

Classification name
Lacrimal Stents And Intubation Sets
Device class
Unclassified
Advisory panel
Unknown
Total cleared
31
First cleared
Most recent

FDA classification definition

“Lacrimal stents and intubations sets are intended to repair the lacrimal drainage system. Lacrimal stents and intubations sets are indicated for, but limited to, the treatment of epiphora in infants and adults; canalicular pathologies such as stenosis; obstruction or laceration; and conditions requiring dacryocystorhinostomy (conventional or laser); or imperforation of the nasolacrimal duct in an infant.”

— U.S. Food and Drug Administration, device classification record for product code OKS, via openFDA

Market context for product code OKS

FDA has cleared 31 devices under product code OKS between 1988 and 2021, filed by 19 applicant companies. No FDA device recalls reference this product code.

Clearances per year

last 15 years

Top applicants under product code OKS

Recent clearances under product code OKS

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