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Innesis Peek Tl Cage

FDA UDI

Class II (US FDA UDI)

by Bk Meditech Co., Ltd.

Identity

Trade Name
INNESIS PEEK TL CAGE FDA UDI
Generic Name
Polymeric spinal interbody fusion cage FDA UDI
Device Name
PEEK Cage, L28 x W10 x H10mm, 0° FDA UDI
Model / Reference
46110 FDA UDI
Description
PEEK Cage, L28 x W10 x H10mm, 0° FDA UDI

Identifiers

Primary DI / UDI-DI
08809228124084 FDA UDI
510(k) Number
K140577 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3080 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: Polymeric spinal interbody fusion cage

Innesis Peek Tl Cage by Bk Meditech Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7af9ce7e-1f96-4373-8a77-a40334fc75a6 34 fields · synced May 30, 2026