510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K170722Substantially Equivalent

Moxxly Flow Collection System

Moxxly, Inc., San Francisco CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K170722 is the FDA 510(k) clearance record for Moxxly Flow Collection System, a class II device, cleared for Moxxly, Inc. on under FDA product code HGX (Pump, Breast, Powered). FDA records list one 510(k) clearance for Moxxly, Inc. As of , FDA records show no recalls naming K170722.

Clearance record

Decision date
Received
(172 days to decision)
Product code
HGX Pump, Breast, Powered
Regulation
21 CFR 884.5160
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Moxxly, Inc. 1777 Yosemite Ave. Suite 235, San Francisco CA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HGX

Trailing 12 months
37 clearances under product code HGX in the twelve months to October 2026, April 2026 the highest month at 8.
Show the numbers
Monthly 510(k) clearances under FDA product code HGX, trailing twelve months
MonthClearances
November 20251
December 20253
January 20261
February 20264
March 20262
April 20268
May 20263
June 20268
July 20262
August 20262
September 20263
October 20260