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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 4 of 57
DeviceModel / ReferenceRegistriesClassStatus
Rayshield LG-FRAK
FDA UDI
Class IActive
ComfortLite LP-CX100
FDA UDI
Class IActive
Aadco SC-720
FDA UDI
Class IActive
Aadco SU-608
FDA UDI
Class IActive
Aadco PB-601
FDA UDI
Class IActive
Hercules OS-31
FDA UDI
Class IActive
ComfortLite LP-CL688
FDA UDI
Class IActive
Rayshield TP-930
FDA UDI
Class IActive
X-Drape D-07N
FDA UDI
Class IActive
Rayshield LP-033
FDA UDI
Class IActive
Hercules OS-645S
FDA UDI
Class IActive
ErgoLite LP-EF601
FDA UDI
Class IActive
X-Drape D-112
FDA UDI
Class IActive
MRI-Safe OSP-511LXNF
FDA UDI
Class IActive
Rayshield TP-909LS
FDA UDI
Class IActive
Rayshield LG-621BM
FDA UDI
Class IActive
Rayshield TP-546S
FDA UDI
Class IActive
Rayshield TP-947
FDA UDI
Class IActive
Rayshield LP-F602
FDA UDI
Class IActive
ComfortLite LP-CA683
FDA UDI
Class IActive
RayShield LP-A903
FDA UDI
Class IActive
ComfortLite LP-CL700-5
FDA UDI
Class IActive
Aadco OSP-445YS
FDA UDI
Class IActive
ComfortLite LP-CX430
FDA UDI
Class IActive
Rayshield LP-F488
FDA UDI
Class IActive
Rayshield LP-F702
FDA UDI
Class IActive
Rayshield TP-949S
FDA UDI
Class IActive
Rayshield LG-2001
FDA UDI
Class IActive
Rayshield S-690
FDA UDI
Class IActive
Aadco N-216
FDA UDI
Class IIActive
ComfortLite LP-CX705-5
FDA UDI
Class IActive
Aadco S-625P
FDA UDI
Class IActive
Aadco SC-774
FDA UDI
Class IActive
ComfortLite LP-CA203
FDA UDI
Class IActive
MRI-Safe NF-120
FDA UDI
Class IActive
Aadco SC-750
FDA UDI
Class IActive
ComfortLite LP-C802C
FDA UDI
Class IActive
RayShield LP-A607
FDA UDI
Class IActive
Rayshield TP-957LS
FDA UDI
Class IActive
Rayshield LP-F902
FDA UDI
Class IActive
Aadco OSP-754WOPC
FDA UDI
Class IActive
ComfortLite LP-CA409
FDA UDI
Class IActive
Hercules OS-634R
FDA UDI
Class IActive
X-Drape D-112GAE
FDA UDI
Class IActive
ErgoLite LP-EL680
FDA UDI
Class IActive
Aadco OSP-10PC
FDA UDI
Class IActive
Aadco OSP-12-SA-B4
FDA UDI
Class IActive
Aadco LP-207
FDA UDI
Class IActive
Aadco PB-108
FDA UDI
Class IActive
Aadco N-215
FDA UDI
Class IIActive

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