510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K852384Substantially Equivalent

Sight Saver All Purpose Lens Carrying Case

Bausch & Lomb Incorporated, Rochester NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K852384 is the FDA 510(k) clearance record for SIGHT SAVER ALL PURPOSE LENS CARRYING CASE, cleared for Bausch & Lomb, Inc. on under FDA product code HPX (Lens, Contact (Polymethylmethacrylate)). FDA records list 131 510(k) clearances for Bausch & Lomb Incorporated, from to . As of , FDA records show no recalls naming K852384.

Clearance record

Decision date
Received
(56 days to decision)
Product code
HPX Lens, Contact (Polymethylmethacrylate)
Device class
Unclassified
Review panel
Unknown
Applicant
Bausch & Lomb, Inc. 1400 N. Goodman St., Rochester NY
Third party review
No

Clearances, product code HPX

Trailing 12 months

FDA records hold no clearances under product code HPX in the trailing twelve months.

FDA records show no clearances under product code HPX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code HPX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260