510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K012830Substantially Equivalent

Lerman & Son Cranial Orthosis Helmet

Lerman & Son, Beverly Hills CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K012830 is the FDA 510(k) clearance record for LERMAN & SON CRANIAL ORTHOSIS HELMET, a class II device, cleared for Lerman & Son on under FDA product code MVA (Orthosis, Cranial). FDA records list one 510(k) clearance for Lerman & Son. As of , FDA records show no recalls naming K012830.

Clearance record

Decision date
Received
(89 days to decision)
Product code
MVA Orthosis, Cranial
Regulation
21 CFR 882.5970
Device class
Class II
Review panel
Neurology
Applicant
Lerman & Son 8710 Wilshire Blvd., Beverly Hills CA
510(k) summary
Summary
Third party review
No

Clearances, product code MVA

Trailing 12 months

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

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