Orthros MIS

FDA UDI

Class II (US FDA UDI)

by Camber Spine Technologies

Identity

Trade Name: Orthros MIS FDA UDI
Generic Name: Polymeric spinal interbody fusion cage FDA UDI
Device Name: Ø5.5mm Curved Rod 55mm Lg FDA UDI
Model / Reference: ORM-55C FDA UDI
Description: Ø5.5mm Curved Rod 55mm Lg FDA UDI

Identifiers

Primary DI / UDI-DI: B030ORM55C0 FDA UDI
FDA Product Code: NKB FDA UDI
KWQ FDA UDI
MNH FDA UDI
MNI FDA UDI
GMDN Term: Polymeric spinal interbody fusion cage FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3070 FDA UDI
888.3060 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Length — 55 Millimeter FDA UDI
Outer Diameter — 5.5 Millimeter FDA UDI

Category: Polymeric spinal interbody fusion cage

Orthros MIS by Camber Spine Technologies — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polymeric spinal interbody fusion cage.

L-Box® — Innovasis, Inc. · Class II
CoRoent — Nuvasive, Inc. · Class II
Novel Spinal Spacer System — ALPHATEC SPINE, INC. · Class II
S-LIFT® — SPINEFRONTIER, INC. · Class II
Peridot Intervertebral body fusion system — GBS Commonwealth Co., Ltd. · Class II
TAURUS PEEK Cage System — Medyssey Co., Ltd. · Class II
Cross-Fuse® II PEEK IBF System — Rti Surgical, Inc. · Class II
Kyocera Medical Technologies, Inc. — Kyocera Medical Technologies, Inc. · Class II

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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Camber Spine Technologies

Sources (1)

FDA UDI 83c5d088-10be-4420-ae07-8346a955e037 35 fields · synced Jun 1, 2026