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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 3 of 57
DeviceModel / ReferenceRegistriesClassStatus
MRI-Safe OS-25NF
FDA UDI
Class IActive
MRI-Safe OS-7601NF
FDA UDI
Class IActive
ErgoLite LP-EX801CA
FDA UDI
Class IActive
ComfortLite LP-CX450
FDA UDI
Class IActive
ComfortLite LP-CA406
FDA UDI
Class IActive
ErgoLite LP-EAV680
FDA UDI
Class IActive
Aadco SC-781
FDA UDI
Class IActive
X-Drape D-116
FDA UDI
Class IActive
ErgoLite LP-EA706
FDA UDI
Class IActive
ComfortLite LP-CX400
FDA UDI
Class IActive
Rayshield TP-908C
FDA UDI
Class IActive
X-Drape D-130G
FDA UDI
Class IActive
Rayshield LP-L702
FDA UDI
Class IActive
Aadco OSP-70-COMM
FDA UDI
Class IActive
Aadco DB-210E
FDA UDI
Class IActive
Aadco PB-159
FDA UDI
Class IActive
Aadco PB-210
FDA UDI
Class IActive
RayShield LP-A951
FDA UDI
Class IActive
ComfortLite LP-CL701
FDA UDI
Class IActive
Rayshield LP-X409
FDA UDI
Class IActive
Rayshield LP-F444K
FDA UDI
Class IActive
ComfortLite LP-CL205
FDA UDI
Class IActive
ComfortLite LP-CF601
FDA UDI
Class IActive
RayShield LP-A103
FDA UDI
Class IActive
Rayshield LP-804
FDA UDI
Class IActive
Aadco OSP-12-EA7
FDA UDI
Class IActive
ComfortLite LP-CA951
FDA UDI
Class IActive
ComfortLite LP-CX688
FDA UDI
Class IActive
Aadco T-1900A
FDA UDI
Class IIActive
Aadco LP-207E
FDA UDI
Class IActive
Rayshield TP-919C
FDA UDI
Class IActive
Aadco GL-2280
FDA UDI
Class IActive
Rayshield TP-903
FDA UDI
Class IActive
X-Drape D-100GA
FDA UDI
Class IActive
RayShield LP-A703
FDA UDI
Class IActive
Aadco OSP-31
FDA UDI
Class IActive
X-Drape D-110
FDA UDI
Class IActive
Rayshield LP-F108
FDA UDI
Class IActive
Rayshield TP-960
FDA UDI
Class IActive
Aadco OSP-7601PC
FDA UDI
Class IActive
ErgoLite LP-EX801A
FDA UDI
Class IActive
Hercules OS-60
FDA UDI
Class IActive
Aadco OSP-8128EC
FDA UDI
Class IActive
Rayshield LP-F684
FDA UDI
Class IActive
Rayshield TP-947S
FDA UDI
Class IActive
Rayshield TP-951C
FDA UDI
Class IActive
Aadco P-306
FDA UDI
Class IActive
ComfortLite LP-CX601
FDA UDI
Class IActive
ComfortLite LP-CL703-5
FDA UDI
Class IActive
ComfortLite LP-CX601-5
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