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Advance Medical Designs, Inc.

United States·US-MF-000009790

Last updated September 17, 2026

About

Trust Advance Medical Designs for innovative surgical infection control. High-quality products and solutions designed for superior OR patient safety.

From the manufacturer's own website. Source

What Advance Medical Designs, Inc. makes

The company manufactures single-use sterile drapes and covers for medical instruments and equipment, including surgical drapes, handle covers, and CO₂ tank covers. It also produces extracorporeal circuit waste bags, in-line arterial blood sampling sets, surgical irrigators, needle guides, and general-purpose fluid transfer sets.

These products are classified as Class I or Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The company is based in the United States.

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

Frequently asked questions

What types of medical devices does Advance Medical Designs, Inc. manufacture?

Advance Medical Designs, Inc. specializes in single-use, sterile medical devices primarily focused on infection control and surgical safety. Their products include instrument/equipment drapes, medical equipment handle covers, surgical drapes, extracorporeal circuit waste bags, in-line arterial blood sampling sets, surgical fluid/gas irrigators, needle guides, and general-purpose fluid transfer sets. These items are designed to minimize contamination risks during medical procedures.

Where is Advance Medical Designs, Inc. based, and what regulatory databases list its devices?

Advance Medical Designs, Inc. is based in the United States. Their devices are listed in the FDA’s Unique Device Identifier (UDI) database, which serves as a centralized registry for tracking medical devices authorized for use in the U.S. This database helps healthcare providers and regulators identify and verify the devices in circulation.

How are the devices manufactured by Advance Medical Designs, Inc. classified under FDA regulations?

The devices produced by Advance Medical Designs, Inc. fall under two primary classifications: Class I and Class II. Class I devices generally pose minimal risk and may require less regulatory oversight, while Class II devices involve a higher level of risk and require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s intended use, potential risks, and the body part or condition it addresses.

Why are the devices from Advance Medical Designs, Inc. listed as single-use?

The devices from Advance Medical Designs, Inc. are designed as single-use to ensure patient safety and infection control. Single-use items are intended for one-time use and disposal after a single procedure, reducing the risk of cross-contamination between patients. This approach aligns with best practices in healthcare to minimize the spread of infections and maintain sterile environments during medical treatments.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
United States
Address
1241 Atlanta Industrial Drive, Marietta, United States
Phone
1 (770) 422 3125
PRRC Contact
David Mackie
EUDAMED SRN
US-MF-000009790
FDA FEI Number
1037885
DUNS Number
—

Catalogue (871)

Page 2 of 18
DeviceModel / ReferenceRegistriesClassStatus
Groin Shield Cover 08-CC138
FDA UDI
Class IIActive
Unbranded GL900NS
FDA UDI
Class IIActive
Sterile Equipment Cover 08-CC233
FDA UDI
Class IIActive
Custom Cover CC602NS
FDA UDI
Class IIActive
Soft Flex Probe Cover 20-PC348
FDA UDI
Class IIActive
Ultrasound Probe Cover Biopsy Needle Guide 28-GG219
FDA UDI
Class IIActive
Custom Pack 08-PK107
FDA UDI
Class IIActive
Slush Drape with Disk 40-SD320
FDA UDI
Class IIActive
Unbranded 06-LK602
FDA UDI
Class IIActive
Drape Sheet SYN-0918
FDA UDI
Class IIActive
Unbranded 06-LK301
FDA UDI
Class IIActive
Snap Kover 02-5090TL
FDA UDI
Class IIActive
Unbranded 09-GL901S
FDA UDI
Class IIActive
Ultrasound Probe Cover Biopsy Needle Guide 28-GG521
FDA UDI
Class IIActive
Unbranded FW3036NS
FDA UDI
Class IIActive
Custom Cover 08-CC152
FDA UDI
Class IIActive
Unbranded CC222NS
FDA UDI
Class IIActive
Unbranded KP14LNS
FDA UDI
Class IIActive
Unbranded FS1430NS
FDA UDI
Class IIActive
Unbranded 09-MK903
FDA UDI
Class IIActive
Unbranded 25-FF648
FDA UDI
Class IIActive
Unbranded 3640-04NS
FDA UDI
Class IIActive
Unbranded 25-FF324
FDA UDI
Class IIActive
Unbranded JA-5313
FDA UDI
Class IIActive
Unbranded 07-HK112
FDA UDI
Class IIActive
Unbranded 02-3640TL
FDA UDI
Class IIActive
Unbranded 09-GL901
FDA UDI
Class IIActive
Ultrasound Probe Cover Biopsy Needle Guide Kit 28-EG143
FDA UDI
Class IIActive
Unbranded 02-4060TL
FDA UDI
Class IIActive
Unbranded 07-PK800
FDA UDI
Class IIActive
Unbranded 09-GL903
FDA UDI
Class IIActive
Unbranded 2217-04
FDA UDI
Class IIActive
Unbranded 01-1010
FDA UDI
Class IIActive
Camera Cover 04-CC220T
FDA UDI
Class IIActive
Drape Sheet SYN-0796
FDA UDI
Class IIActive
Unbranded 09-MK901
FDA UDI
Class IIActive
Unbranded 20-PC648
FDA UDI
Class IIActive
Camera Cover 08-CC149
FDA UDI
Class IIActive
Leap Med 28-TPUA170
FDA UDI
Class IActive
Custom Cover 08-CC139
FDA UDI
Class IIActive
Easy Catcher O-EC52-UK
FDA UDI
Class IIActive
Unbranded HP48RNS
FDA UDI
Class IIActive
9600/9800/9900 Super C 12" 5254382
FDA UDI
Class IIActive
Transducer Cover 05-TC996
FDA UDI
Class IIActive
Unbranded 63-PM48M
FDA UDI
Class IIActive
Unbranded KP18LNS
FDA UDI
Class IIActive
Unbranded 07-CA300
FDA UDI
Class IIActive
Custom Drape w/o Rubber Bands 08-CC147
FDA UDI
Class IIActive
Unbranded 62-PM06F
FDA UDI
Class IIActive
Micro Kover 09-MK981
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

Importers

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Notified Bodies

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Authorities

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FDA Recalls (7)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Advance Medical Designs, Inc. has seven FDA recall records, with the earliest initiated on June 18, 2004, and the most recent on July 7, 2023. The records reflect recalls with statuses marked as open, classified, and terminated. The reasons cited include mislabeling of ultrasound gel regarding inappropriate use and a potential structural failure where the product may detach when excessive force is applied to the coupler.

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
Jul 7, 2023Z-2532-2023—open, classified

Ultrasound gel mislabeled with inappropriate use.

Jul 7, 2023Z-2537-2023—open, classified

Ultrasound gel mislabeled with inappropriate use.

Jul 7, 2023Z-2536-2023—open, classified

Ultrasound gel mislabeled with inappropriate use.

Jul 7, 2023Z-2533-2023—open, classified

Ultrasound gel mislabeled with inappropriate use.

Jul 7, 2023Z-2535-2023—open, classified

Ultrasound gel mislabeled with inappropriate use.

Jul 7, 2023Z-2534-2023—open, classified

Ultrasound gel mislabeled with inappropriate use.

Jun 18, 2004Z-1036-04—terminated

The product may come apart when excessive force is applied to the coupler.