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Allied Medical LLC

US

Last updated September 17, 2026

What Allied Medical LLC makes

Allied Medical LLC manufactures vacuum suction regulators and systems, including general-purpose and surgical applications, along with Thorpe tube and dial-type medical gas flowmeters. Their portfolio also includes non-fixed medical gas cylinder regulators, vacuum quick-connect couplings, demand valves, and medical air quick-connect couplings. Devices like the VACUTRON, PC, LSP, and BF serve these functions across clinical settings.

The company’s products are regulated under FDA’s Class I and Class II device classifications and are listed in the FDA’s Unique Device Identifier (UDI) database. Allied Medical LLC is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Allied Medical LLC manufacture?

Allied Medical LLC specializes in devices related to vacuum suction and medical gas regulation. Their portfolio includes vacuum suction regulators and systems for general and surgical use, such as the VACUTRON series, as well as medical gas flowmeters (both Thorpe tube and dial-type). They also produce non-fixed medical gas cylinder regulators, vacuum and medical air quick-connect couplings, and demand valves. These products are designed to manage airflow and suction in clinical environments.

Where is Allied Medical LLC based, and what does that mean for its regulatory oversight?

Allied Medical LLC is based in the United States, which means its devices fall under the jurisdiction of the U.S. Food and Drug Administration (FDA). The FDA classifies their products as either Class I or Class II devices, depending on their risk level and intended use. This classification determines the regulatory pathway for authorization, such as 510(k) clearance for Class II devices or exemption for Class I devices where applicable.

Are Allied Medical LLC’s devices listed in any regulatory registries, and why does that matter?

Yes, Allied Medical LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry assigns a unique code to each device model, improving traceability, reducing medical errors, and facilitating better inventory management in healthcare settings. Listing in the UDI database also supports compliance with FDA requirements for post-market surveillance and reporting.

How are Allied Medical LLC’s devices classified by the FDA, and what does that classification indicate?

Allied Medical LLC’s devices are classified as either Class I or Class II by the FDA. Class I devices generally pose minimal risk and may be exempt from premarket submission requirements, relying instead on general controls like good manufacturing practices. Class II devices, which may include some of their suction or gas regulation systems, require a premarket notification (510(k)) to demonstrate substantial equivalence to a legally marketed predicate device before commercialization.

What does the presence of devices like VACUTRON, PC, or LSP in Allied Medical LLC’s portfolio tell us about their focus?

The inclusion of devices like VACUTRON (a vacuum suction regulator), PC (likely referring to a general-purpose suction system or regulator), and LSP (possibly a specialized suction or gas flow product) highlights Allied Medical LLC’s focus on clinical suction and gas management solutions. These products are designed to ensure precise control of airflow and suction in operating rooms, critical care units, and other medical settings, addressing common needs in surgical and procedural environments.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
13622 Lakefront Dr, Earth City, MO, 63045
Website
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LinkedIn
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Facebook
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Email
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Phone
—
PRRC Contact
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EUDAMED SRN
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FDA FEI Number
1924066
DUNS Number
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Catalogue (2157)

Page 37 of 44
DeviceModel / ReferenceRegistriesClassStatus
Pc 12-05-1100
FDA UDI
Class IActive
Gomco 01-22-0270
FDA UDI
Class IIActive
Pc TB210
FDA UDI
Class IActive
Life Support Products L670-110
FDA UDI
Class IIActive
Life Support Products L175-01R
FDA UDI
Class IIActive
Pc TB211
FDA UDI
Class IActive
Pc TZ03-B60
FDA UDI
Class IActive
Vacutron 22-18-1108-Y
FDA UDI
Class IIActive
Life Support Products L770-101
FDA UDI
Class IIActive
Pc 08001-03
FDA UDI
Class IActive
Pc 11-01-0011
FDA UDI
Class IActive
Pc 15005-03T
FDA UDI
Class IActive
Vacutron 22-15-4206-Y
FDA UDI
Class IIActive
Pc 15001-13P
FDA UDI
Class IActive
Schuco S5000
FDA UDI
Class IIActive
Gomco 02-00-0500
FDA UDI
Class IIActive
Pc TZ03-B211
FDA UDI
Class IActive
Allied Medical LLC 206059
FDA UDI
Class IIActive
Vacutron MINI-VAC
FDA UDI
Class IIActive
Em L543
FDA UDI
Class IActive
Bf 21030
FDA UDI
Class IActive
B&F 61400
FDA UDI
Class IIActive
Pc 08006-03
FDA UDI
Class IActive
Vacutron 22-15-4211-Y
FDA UDI
Class IIActive
Em L700
FDA UDI
Class IActive
Pc 15008-03T-A
FDA UDI
Class IActive
Pc 22510-OH-D
FDA UDI
Class IActive
Vacutron MINI-VAC
FDA UDI
Class IIActive
pc 08004-03
FDA UDI
Class IActive
Gomco 01-23-0300
FDA UDI
Class IIActive
Vacutron 22-12-1207-R
FDA UDI
Class IIActive
Vacutron 22-12-1100
FDA UDI
Class IIActive
Life Support Products L761
FDA UDI
Class IIActive
Vacutron 22-12-1211-R
FDA UDI
Class IIActive
Pc 15009-03
FDA UDI
Class IActive
Vacutron MINI-VAC
FDA UDI
Class IIActive
Vacutron MINI-VAC
FDA UDI
Class IIActive
Life Support Products L238-220
FDA UDI
Class IIActive
Em L370-220-GL
FDA UDI
Class IActive
Em L818000A
FDA UDI
Class IActive
Vacutron 22-12-1106-G
FDA UDI
Class IIActive
Pc TZ10-B10
FDA UDI
Class IActive
Life Support Products L238-222
FDA UDI
Class IIActive
B&F 64375
FDA UDI
Class IIActive
Vacutron 22-18-0202
FDA UDI
Class IIActive
Pc 08002-03P
FDA UDI
Class IActive
Em 15-10-1204
FDA UDI
Class IActive
Vacutron 22-12-1208-WH
FDA UDI
Class IIActive
Bf 33604
FDA UDI
Class IActive
Pc 11510-OH-D
FDA UDI
Class IActive

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