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AADCO MEDICAL, INC.

US

Last updated September 17, 2026

What AADCO MEDICAL, INC. makes

AADCO Medical, Inc. manufactures radiation shielding products, including reusable and single-use items like aprons, goggles, and drapes designed to protect patients and staff from ionizing radiation. Their portfolio also includes custom medical device mounts, freestanding patient positioners, and fixed or portable shielding panels for radiological and surgical settings. Positioning devices for general body-part radiography are also part of their offerings.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identification (UDI) database. Their products are regulated under U.S. medical device laws, with compliance requirements varying by class. The manufacturer is based in the United States.

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

Information

Country
US
Address
2279 Vermont Route 66, RANDOLPH, VT, 05060
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
3001237319
DUNS Number
153603204

Catalogue (2842)

Page 53 of 57
DeviceModel / ReferenceRegistriesClassStatus
Rayshield LP-L607
FDA UDI
Class IActive
ComfortLite LP-CF953
FDA UDI
Class IActive
Hercules OS-665R
FDA UDI
Class IActive
ComfortLite LP-CF104
FDA UDI
Class IActive
Aadco PB-175C
FDA UDI
Class IActive
ComfortLite LP-CX707
FDA UDI
Class IActive
Aadco SC-763
FDA UDI
Class IActive
X-Drape D-111
FDA UDI
Class IActive
Aadco PB-206
FDA UDI
Class IActive
Aadco P-137C
FDA UDI
Class IActive
ComfortLite LP-CX689
FDA UDI
Class IActive
ComfortLite LP-CA902
FDA UDI
Class IActive
Rayshield LG-900B
FDA UDI
Class IActive
Hercules OS-888CT
FDA UDI
Class IActive
Rayshield TP-600
FDA UDI
Class IActive
Hercules OSL-201
FDA UDI
Class IActive
Rayshield LP-F666V
FDA UDI
Class IActive
Rayshield LP-X666K
FDA UDI
Class IActive
Hercules OS-11-3
FDA UDI
Class IActive
ErgoLite LP-EX205
FDA UDI
Class IActive
ComfortLite LP-C802CA
FDA UDI
Class IActive
ComfortLite LP-CL444K
FDA UDI
Class IActive
ComfortLite LP-CL953
FDA UDI
Class IActive
Rayshield LP-L901
FDA UDI
Class IActive
ComfortLite LP-CA606
FDA UDI
Class IActive
Rayshield LP-813
FDA UDI
Class IActive
ErgoLite LP-EX452
FDA UDI
Class IActive
Rayshield TP-929LS
FDA UDI
Class IActive
ComfortLite LP-CA438
FDA UDI
Class IActive
ErgoLite LP-EF701
FDA UDI
Class IActive
Rayshield TP-921P
FDA UDI
Class IActive
MRI-Safe OSP-CBNF
FDA UDI
Class IActive
Hercules OS-10
FDA UDI
Class IActive
ErgoLite LP-EA202
FDA UDI
Class IActive
ErgoLite LP-EA206
FDA UDI
Class IActive
ComfortLite LP-CA609-5
FDA UDI
Class IActive
MRI-Safe NF-533
FDA UDI
Class IActive
Hercules OS-568N
FDA UDI
Class IActive
Rayshield LG-ATTTT
FDA UDI
Class IActive
Rayshield LP-L804
FDA UDI
Class IActive
Rayshield LP-X904
FDA UDI
Class IActive
Rayshield TP-845P
FDA UDI
Class IActive
Rayshield TP-915
FDA UDI
Class IActive
MRI-Safe OS-888PNF
FDA UDI
Class IActive
Rayshield LG-701B
FDA UDI
Class IActive
Hercules OSL-211
FDA UDI
Class IActive
ErgoLite LP-EF683
FDA UDI
Class IActive
Rayshield LP-X206
FDA UDI
Class IActive
ErgoLite LP-EF777
FDA UDI
Class IActive
Hercules OSP-10S
FDA UDI
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.

AADCO Medical, Inc. has one FDA recall record initiated on November 1, 2007, which is recorded as terminated. The recall was due to the potential for screws to become loose from the mounted shield, which could compromise stability.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

DateRecall No.ClassStatusReason
Nov 1, 2007Z-0552-2008—terminated

Screws may become loose from the mounted shield compromising stability