ARCH Medical Solutions - Memphis

FDA registration

ARCH Medical Solutions - Memphis·2 products·🇺🇸 United States

ARCH Medical Solutions - Memphis

FDA registration

ARCH Medical Solutions - Memphis·2 products·🇺🇸 United States

INDEPENDENCE Spacers, HEDRON IA, MAGNIFY-S Spacers, MONUMENT Spacers, InterContinental Plate-Spacer, ELSA Spacers

FDA 510(k)

FDA Class 2 ·Orthopedic

16M - Navajo Tribal Utility Authority - Metal

FDA UDI

Certified Safety Manufacturing, Inc.·00766588012780·16M - Navajo Tribal Utility Authority - Metal

Ophthalmic Cannula

FDA UDI

KATENA PRODUCTS, INC.·00841668114254·CHAMBER MAINTAINER 25GA (PK/10)

Ophthalmic Cannula

FDA UDI

KATENA PRODUCTS, INC.·00841668114261·CHAMBER MAINTAINER 23GA (PK/10)

CytoCore

FDA registration

PRAXIS MEDICAL LLC·1 product·🇺🇸 United States

Praxis9151 (LN) - CytoCore

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

Assure Prism Control Solution

FDA registration

I-SENS, INC.·3 products·🇰🇷 South Korea

Assure Prism Control Solution

FDA registration

i-SENS Wonju Factory·3 products·🇰🇷 South Korea

INSERT MOLDING SOLUTIONS, INC.

FDA registration

INSERT MOLDING SOLUTIONS, INC.·1 product·🇺🇸 United States

Albumin BCG2 (ARCHITECT, LN 04T3420 and 04T3430)

FDA registration

ABBOTT GmbH·1 product·🇩🇪 Germany

Albumin BCG2 (ARCHITECT, LN 04T3420 and 04T3430)

FDA registration

ABBOTT IRELAND DIAGNOSTICS DIVISION·1 product·🇮🇪 Ireland

Boston Scientific Corp., Marina Bay Cust. Fulfillment Center

FDA registration

Boston Scientific Corp., Marina Bay Cust. Fulfillment Center·4 products·🇺🇸 United States

Boston Scientific Corporation

FDA registration

Boston Scientific Corporation·4 products·🇺🇸 United States

BOMEI CO., LTD.

FDA registration

BOMEI CO., LTD.·1 product·🇹🇼 Taiwan

ACURA PLUS BLOOD GLUCOSE MONITORING SYSTEM; ACURA PLUS BLOOD GLUCOSE METER; ACURA CONTROL SOLUTION

FDA 510(k)

FDA Class 2 ·Clinical Chemistry

COMPLETE HUMAN TUBAL FLUID (HTF) WITH SERUM SUBSTITUTE SUPPLEMENT, MODEL 9922

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Media, Reproductive

FDA classification

FDA Class 2 ·Media, Reproductive