Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029755538

FEI Number

3029755538

Entity Name

ASMOH USA INC

City/State/Country

Sunrise, FL, US

Establishment Address

12054 Miramar PRWY, Sunrise, FL 33325, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

ASMOH USA INC (Owner Number: 10089012)

Owner / Operator Contact Address

200 N COMMERCE PARKWAY SUITE # 200, Weston, FL 33326, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K210103

PMA Number

N/A

All Registered Proprietary Names

ASMOH SYRINGES AND SAFETY NEEDLES

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FMF	Syringe, Piston	General Hospital	Class 2	880.5860	2024-03-14
MEG	Syringe, Antistick	General Hospital	Class 2	880.5860	2024-03-14
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2024-03-14
FMF	Syringe, Piston	General Hospital	Class 2	880.5860	2024-03-14
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2024-03-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ASMOH USA INC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K880350	Honway International Co.	YUE/FA DISPOSABLE SYRINGE	1988-02-16
K003571	Terumo Medical Corp.	SERONO FOR USE WITH GONAL-F 1200IU MULTI-DOSE ONLY AT 600IU/ML SYRINGE	2001-02-12
K092413	Inviro Medical Devices, Inc.	INVIROSNAP 50 AND 100 UNIT INSULIN SAFETY SYRINGES	2009-09-04
K163162	Jiangxi Hongda Medical Equipment Group , Ltd.	Sterile Hypodermic Safety Syringes for Single Use	2017-03-20
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0003-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 30G X 5/16'' syringes
Z-0004-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1 cc X 29G X 1/2 '' insulin syringes
Z-0005-04	Liberty Medical Supplies	2	Liberty brand Insulin Syringes for use with U-100 insulin, 1/2 cc X 29G X 1/2 '' insulin syringes
Z-0005-2024	Fresenius Medical Care Holdings, Inc.	2	10ML SYRINGE LUER LOCK W/OUT NEEDLE, Part Number 15-R010-0, 100 per box, 12 boxes to a case
Z-0006-2024	Fresenius Medical Care Holdings, Inc.	2	10ML SYRINGE LUER LOCK W/NEEDLE, Part Number 15-10ML-0, 100 per box, 12 boxes per case

Similar Registrations

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3009249481	JMS Co.,Ltd. Miyoshi Plant	Miyoshi Hiroshima, JP
1416980	BAXTER HEALTHCARE CORPORATION	ROUND LAKE, IL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3029755538. Last updated year: 2026. Please use registration number 3029755538 when referencing this establishment in official correspondence.