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Blue Sky Bio, LLC.

FDA UDI

Class II (US FDA UDI)

by Blue Sky Bio Llc

Identity

Trade Name
Blue Sky Bio, LLC. FDA UDI
Generic Name
Screw endosteal dental implant, two-piece FDA UDI
Device Name
BIO | Internal Hex Cobalt Base Abutment 3.5 Platform FDA UDI
Model / Reference
ABCIH35 FDA UDI
Description
BIO | Internal Hex Cobalt Base Abutment 3.5 Platform FDA UDI

Identifiers

Primary DI / UDI-DI
00810060224694 FDA UDI
510(k) Number
K202026 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Screw endosteal dental implant, two-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Screw endosteal dental implant, two-piece

Blue Sky Bio, LLC. by Blue Sky Bio Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Screw endosteal dental implant, two-piece.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Blue Sky Bio Llc

Sources (1)

  • FDA UDI d4e97281-eff3-4a35-b651-50f2dfc35929 34 fields · synced May 30, 2026