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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 7 of 57
DeviceModel / ReferenceRegistriesClassStatus
Rayshield TP-974
FDA UDI
Class IActive
ErgoLite LP-EF680
FDA UDI
Class IActive
ErgoLite LP-EA608
FDA UDI
Class IActive
Rayshield TP-236
FDA UDI
Class IActive
Rayshield TP-725
FDA UDI
Class IActive
Aadco S-305
FDA UDI
Class IActive
ErgoLite LP-EX204
FDA UDI
Class IActive
Hercules OS-1-754E
FDA UDI
Class IActive
Hercules OS-701
FDA UDI
Class IActive
Aadco OSP-10SS
FDA UDI
Class IActive
ComfortLite LP-CX702
FDA UDI
Class IActive
Hercules OS-745/OSP-260
FDA UDI
Class IActive
Aadco SC-999
FDA UDI
Class IActive
ComfortLite LP-CX706
FDA UDI
Class IActive
Rayshield TP-1010B
FDA UDI
Class IActive
Rayshield TP-911
FDA UDI
Class IActive
Hercules OS-12
FDA UDI
Class IActive
ComfortLite LP-CX608
FDA UDI
Class IActive
Rayshield LP-F201
FDA UDI
Class IActive
ComfortLite LP-CF405
FDA UDI
Class IActive
ComfortLite LP-CH860
FDA UDI
Class IActive
ErgoLite LP-EX700
FDA UDI
Class IActive
Rayshield TP-803P
FDA UDI
Class IActive
ErgoLite LP-EA704
FDA UDI
Class IActive
Aadco SC-785
FDA UDI
Class IActive
MRI-Safe OSP-888NF
FDA UDI
Class IActive
Aadco OSP-15EA
FDA UDI
Class IActive
ErgoLite LP-EA207
FDA UDI
Class IActive
ComfortLite LP-C801X
FDA UDI
Class IActive
Hercules OS-11
FDA UDI
Class IActive
Aadco SC-992
FDA UDI
Class IActive
ComfortLite LP-CL950
FDA UDI
Class IUnknown
Aadco DB-6550
FDA UDI
Class IActive
ComfortLite LP-CL402
FDA UDI
Class IActive
Aadco GL-2220
FDA UDI
Class IActive
ComfortLite LP-CX604-5
FDA UDI
Class IActive
ComfortLite LP-CF706
FDA UDI
Class IActive
ComfortLite LP-CA485
FDA UDI
Class IActive
Rayshield TP-952S
FDA UDI
Class IActive
Aadco S-404P
FDA UDI
Class IActive
ErgoLite LP-EXV683
FDA UDI
Class IActive
Hercules OS-645RS
FDA UDI
Class IActive
ErgoLite LP-EX600
FDA UDI
Class IActive
MRI-Safe OS-745RNF
FDA UDI
Class IActive
ComfortLite LP-CL604-5
FDA UDI
Class IActive
Aadco OSP-18AWGG/YW
FDA UDI
Class IActive
Aadco P-200C
FDA UDI
Class IActive
Aadco OSP-AMU1084
FDA UDI
Class IActive
ComfortLite LP-CA702
FDA UDI
Class IActive
ComfortLite LP-CL489
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