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BLUE SKY BIO LLC

United States·US-MF-000014016

Last updated May 24, 2026

What BLUE SKY BIO LLC makes

Blue Sky Bio LLC manufactures dental implant components, including permanent preformed suprastructures, two-piece screw endosteal implants, and reusable fixture/appliance drill bits. Their portfolio also includes dental implant analogs, ceramic fabrication materials for appliances, suprastructure kits, guided surgery reference pins, and torque wrench adaptors for surgical procedures.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. 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.

Frequently asked questions

What types of medical devices does Blue Sky Bio LLC manufacture?

Blue Sky Bio LLC specializes in dental implant-related devices. Their portfolio includes permanent preformed dental implant suprastructures, two-piece screw endosteal dental implants, reusable fixture/appliance drill bits, dental implant analogs, ceramic materials for dental appliance fabrication, suprastructure kits, guided surgery reference pins, and surgical torque wrench adaptors. These products are designed to support dental restoration procedures and surgical precision.

Where is Blue Sky Bio LLC based?

Blue Sky Bio LLC is headquartered in the United States. The company’s location is relevant for regulatory compliance, manufacturing oversight, and customer support related to its dental implant devices.

Which regulatory registries list Blue Sky Bio LLC’s devices?

Blue Sky Bio LLC’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for healthcare providers, ensuring they can verify the identity and regulatory status of the devices in use.

How are Blue Sky Bio LLC’s devices classified under FDA regulations?

Blue Sky Bio LLC’s devices fall under FDA’s Class I and Class II classifications. Class I devices generally pose minimal risk and may require general controls, while Class II devices involve a higher level of risk and may require special controls to ensure safety and effectiveness. The classification depends on factors like the device’s purpose, intended use, and potential risks.

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

Information

Country
United States
Address
800, Liberty Drive, Libertyville, United States
Website
accumedix.com
LinkedIn
—
Facebook
—
Phone
8476822688
PRRC Contact
Michele Kupcso
EUDAMED SRN
US-MF-000014016
FDA FEI Number
—
DUNS Number
618960848

Catalogue (1705)

Page 35 of 35
DeviceModel / ReferenceRegistriesClassStatus
Drill N Implant 4.7 Short DRILL4438S
EUDAMEDFDA UDI
Class IIaActive
Guided Drill 4.6 x 8mm DRILG4608
EUDAMEDFDA UDI
Class IIaActive
BIO | Cut Guide Tube 5.57 OD x 4.52 ID x 4mm L TUBE557-452-4L
EUDAMEDFDA UDI
Class IActive
Bone Condenser 6/7 STPCND67
EUDAMEDFDA UDI
Class IActive
BIO | Guide-Tube Nobel Master Wide 6.09 OD x 4.68 ID TUBE609-468
EUDAMEDFDA UDI
Class IActive

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