510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K992240Substantially Equivalent

Pillar Malar Implant

Pillar Surgical, Inc., La Jolla CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K992240 is the FDA 510(k) clearance record for PILLAR MALAR IMPLANT, a class II device, cleared for Pillar Surgical, Inc. on under FDA product code LZK (Implant, Malar). FDA records list 7 510(k) clearances for Pillar Surgical, Inc., from to . As of , FDA records show no recalls naming K992240.

Clearance record

Decision date
Received
(143 days to decision)
Product code
LZK Implant, Malar
Regulation
21 CFR 878.3550
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Pillar Surgical, Inc. P.O. Box 8141, La Jolla CA
510(k) summary
Summary
Third party review
No

Clearances, product code LZK

Trailing 12 months

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

FDA records show no clearances under product code LZK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LZK, 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