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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 6 of 57
DeviceModel / ReferenceRegistriesClassStatus
Aadco LP-004
FDA UDI
Class IActive
Rayshield TP-805P
FDA UDI
Class IActive
Rayshield LP-F955
FDA UDI
Class IActive
Rayshield LP-031
FDA UDI
Class IActive
MRI-Safe OS-745NF
FDA UDI
Class IActive
ComfortLite LP-CA708
FDA UDI
Class IActive
Rayshield LP-836
FDA UDI
Class IActive
Hercules OSP-766E
FDA UDI
Class IActive
Aadco SC-743
FDA UDI
Class IActive
Aadco NF-276FP
FDA UDI
Class IActive
Aadco PB-220C
FDA UDI
Class IActive
Aadco N-105
FDA UDI
Class IIActive
Aadco PB-118
FDA UDI
Class IActive
Aadco DB-2836E
FDA UDI
Class IActive
Rayshield TP-928S
FDA UDI
Class IActive
ComfortLite LP-CL905
FDA UDI
Class IActive
Hercules OSL-101-7662
FDA UDI
Class IActive
ErgoLite LP-EX430
FDA UDI
Class IActive
Aadco S-311AP
FDA UDI
Class IActive
Rayshield LP-0037
FDA UDI
Class IActive
ErgoLite LP-EFV681
FDA UDI
Class IActive
Rayshield TP-995
FDA UDI
Class IActive
Rayshield TP-928
FDA UDI
Class IActive
ComfortLite LP-CA600-5
FDA UDI
Class IActive
Rayshield TP-913S
FDA UDI
Class IActive
Rayshield TP-927S
FDA UDI
Class IActive
ErgoLite LP-EL600
FDA UDI
Class IActive
Aadco SC-900
FDA UDI
Class IActive
Aadco PB-501U
FDA UDI
Class IActive
ComfortLite LP-CA603-5
FDA UDI
Class IActive
Rayshield LP-X488
FDA UDI
Class IActive
Rayshield TP-924L
FDA UDI
Class IActive
Aadco OSP-7601BW
FDA UDI
Class IActive
Aadco PB-115
FDA UDI
Class IActive
ComfortLite LP-CF407
FDA UDI
Class IActive
Hercules OS-568NC
FDA UDI
Class IActive
Rayshield LP-X107
FDA UDI
Class IActive
Aadco OSP-568NYS
FDA UDI
Class IActive
Aadco PB-186
FDA UDI
Class IActive
Aadco OSP-7601N
FDA UDI
Class IActive
Hercules OS-434R
FDA UDI
Class IActive
Aadco OSP-12CB
FDA UDI
Class IActive
Aadco OSP-596-SYS
FDA UDI
Class IActive
Aadco T-1950
FDA UDI
Class IIActive
Rayshield LG-500ND
FDA UDI
Class IActive
X-Drape D-125NE
FDA UDI
Class IActive
MRI-Safe OSP-766ENF
FDA UDI
Class IActive
Aadco GL-2130-3
FDA UDI
Class IActive
X-Drape D-180E
FDA UDI
Class IActive
Rayshield LP-F407
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