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Alliance Medical, Inc.

US

Last updated May 23, 2026

What Alliance Medical, Inc. makes

Alliance Medical, Inc. manufactures a range of reprocessed orthopedic and surgical devices, including compression sleeves, soft tissue ablators, athroscopic burs, diamond burs, external fixation devices, electrophysiology catheters, and phacoemulsification tips, as well as a disposable sterile drape sheet.

These products are regulated as Class II and Class U medical devices and are listed in the FDA 510(k) database; the company 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 Alliance Medical, Inc. manufacture?

Alliance Medical, Inc. produces reprocessed orthopedic and surgical devices such as compression sleeves, soft‑tissue ablators, arthroscopic and diamond burs, external fixation devices, electrophysiology catheters, phacoemulsification tips, and a disposable sterile drape sheet. This list is taken directly from the provided device data, so no other products are assumed.

Where is Alliance Medical, Inc. located and under which regulatory framework are its devices listed?

The company is based in the United States, as indicated by the COUNTRY field. Its devices appear in the FDA 510(k) database, meaning they are subject to the FDA’s 510(k) premarket submission process. This information comes from the LISTED IN entry in the data.

How are the devices from Alliance Medical, Inc. classified under FDA regulations?

According to the DEVICE CLASSES entry, Alliance Medical’s products are classified as Class II and Class U medical devices. Class II devices are moderate‑risk devices requiring special controls, while Class U denotes unclassified devices that are reviewed on a case‑by‑case basis. This classification is explicitly stated in the data.

Are Alliance Medical, Inc.’s devices approved or cleared by the FDA?

The data only indicates that the devices are listed in the FDA 510(k) database and assigned to Class II or Class U. It does not state that any specific device has received FDA approval, clearance, or certification, and we must not infer such status. Therefore, we can only confirm their regulatory listing, not an approval.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
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Catalogue (73)

Page 1 of 2
DeviceModel / ReferenceRegistriesClassStatus
All Flow 5557100
FDA UDI
Class IIActive
All Flow Valved Insp. Mthpc 3122069
FDA UDI
Class IActive
All Flow 7774100
FDA UDI
Class IIActive
All Flow Mthpc. Adapter 3122220
FDA UDI
Class IActive
All Flow Adult Disp Mthpc. 3122200
FDA UDI
Class IActive
All Flow Peds Disp Mthpc. 3123200
FDA UDI
Class IActive
All Flow 7773100
FDA UDI
Class IIActive
All Flow 5556100
FDA UDI
Class IIActive
All Flow 7771100
FDA UDI
Class IIActive
All Flow Resp. Disp. Mthpc. 3125500
FDA UDI
Class IActive
All Flow 7776100
FDA UDI
Class IIActive
All Flow 5551100
FDA UDI
Class IIActive
All Flow 7778100
FDA UDI
Class IIActive
All Flow 5558100
FDA UDI
Class IIActive
All Flow Thermoplastic Rbr Mthpc. 5550050
FDA UDI
Class IActive
All Flow 5553100
FDA UDI
Class IIActive
All Flow 7775100
FDA UDI
Class IIActive
All Flow 5555100
FDA UDI
Class IIActive
All Flow 5559100
FDA UDI
Class IIActive
InFloCone 1357050
FDA UDI
Class IActive
All Flow 7779100
FDA UDI
Class IIActive
All Flow 7777100
FDA UDI
Class IIActive
All Flow 5554100
FDA UDI
Class IIActive
All Flow Valved Ex.Mthpc. 3122064
FDA UDI
Class IActive
InFloCone-V 1459050
FDA UDI
Class IActive
Alliance Medical Corporation Reprocessed Compression Sleeves K060091
FDA 510(k)
Class IIActive
Reprocessed Soft Tissue Ablators K012631
FDA 510(k)
Class IIActive
Reprocessed Athroscopics Burs K012605
FDA 510(k)
Class IIActive
Reprocessed External Fixation Devices K052918
FDA 510(k)
Class IIActive
Alliance Medical Corporation Reprocessed External Fixation Devices K052064
FDA 510(k)
Class IIActive
Reprocessed Electrophysiology Catheter K030279
FDA 510(k)
Class IIActive
Reprocessed External Fixation Device K023714
FDA 510(k)
Class IIActive
Disposable Ama Sterile Drape Sheet, Cat. No. 5252 K931091
FDA 510(k)
Class IIActive
Reprocessed Electrophysiology Catheters K061045
FDA 510(k)
Class IIActive
Reprocessed Phacoemulsification Tips K060648
FDA 510(k)
Class IIActive
Reprocessed External Fixation Device K012623
FDA 510(k)
Class IIActive
Reprocessed Diamond Burs K041978
FDA 510(k)
Class IIActive
Reprocessed External Fixation Device K012634
FDA 510(k)
Class IIActive
Reprocessed Compression Sleeves K024074
FDA 510(k)
Class IIActive
Reprocessed Linvatec Arthroscopic Burs K012630
FDA 510(k)
Class IIActive
Reprocessed Compression Sleeves K024087
FDA 510(k)
Class IIActive
Reprocessed Electrophysiology Catheter K030187
FDA 510(k)
Class IIActive
Alliance Medical Corporation Reprocessed External Fixation Devices K051554
FDA 510(k)
Class IIActive
Reprocessed Ultrasonic Scalpels K043358
FDA 510(k)
UActive
Reprocessed Electrophysiology Catheter K052414
FDA 510(k)
Class IIActive
Reprocessed Diagnostic Ultrasound Catheter K033436
FDA 510(k)
Class IIActive
Amib7 K990198
FDA 510(k)
Class IIActive
Reprocessed Phacoemuisification Tips K050518
FDA 510(k)
Class IIActive
Alliance Medical Corporation Reprocessed External Fixation Devices K052065
FDA 510(k)
Class IIActive
Electrophysiology Catheter K012708
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Notified Bodies

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Authorities

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Oct 6, 2014Z-0714-2020—completed

Patients have experienced a bad taste associated with the filters.