Vega

FDA UDI

Class II (US FDA UDI)

by OSTEONIC CO., Ltd.

Identity

Trade Name: VEGA FDA UDI
Generic Name: Tendon/ligament bone anchor, bioabsorbable FDA UDI
Model / Reference: CIS0823-BC FDA UDI

Identifiers

Primary DI / UDI-DI: 08800071020875 FDA UDI
510(k) Number: K210122 FDA UDI
FDA Product Code: MAI FDA UDI
GMDN Term: Tendon/ligament bone anchor, bioabsorbable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Tendon/ligament bone anchor, bioabsorbable

Vega by OSTEONIC CO., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tendon/ligament bone anchor, bioabsorbable.

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Arthrex® — Arthrex, Inc. · Class II
5 x 15mm CitreLock Implant — ACUITIVE TECHNOLOGIES · Class II
Fixone Hybrid Anchor — AJU PHARM. CO., LTD. · Class II
RIGIDFIX BIOCRYL — Medos International Sàrl · Class II
Arthrex® — Arthrex, Inc. · Class II

Cleared under the same submission

K210122 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: OSTEONIC CO., Ltd.

Sources (1)

FDA UDI d8230895-40ef-4248-b4fa-23a0e6d61188 33 fields · synced May 30, 2026