Facility

GA HEALTH COMPANY LIMITED

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3014749926
Establishment type	Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Export Device to the United States But Perform No Other Operation on Device
Location	Unit 1511-13 & 15, 15/F, Tower 2, Grand Central Plaza Hong Kong, HK None
Registration status	Active · expires 2026
Parent company	GA Health Company Limited (owner-operator 10061258)
Brand names	aquapulse; ENDO092US; ENDO126US

Activity by year

Recalls (1)

Devices registered here (1)

Endoscopic Irrigation/Suction System
Product code OCX (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.1500

Recalls & enforcement

Class IITerminated2020-11-03
Suction button is reported sticky and/or broken during or after the procedure, may cause prolonged procedure

All facilities operated by GA Health Company Limited

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “GA HEALTH COMPANY LIMITED (FEI 3014749926) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3014749926-ga-health-company-limited/

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