Epiphany

FDA UDI

Class II (US FDA UDI)

by Pantheon Spinal LLC

Identity

Trade Name: Epiphany FDA UDI
Generic Name: Polymeric spinal interbody fusion cage FDA UDI
Device Name: Spann LLIF Cage 60x22x08mm FDA UDI
Model / Reference: 1 FDA UDI
Description: Spann LLIF Cage 60x22x08mm FDA UDI

Identifiers

Catalog Number: LPSL 60-22-08 FDA UDI
Primary DI / UDI-DI: B528LPSL6022080 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

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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Height — 8 Millimeter FDA UDI
Length — 60 Millimeter FDA UDI
Width — 22 Millimeter FDA UDI

Category: Polymeric spinal interbody fusion cage

Intervertebral fusion devices like the Epiphany are designed to provide mechanical stability and sufficient space for therapeutic spinal bone fusion to occur. These devices feature a hollow, porous, threaded and/or fenestrated cylindrical or geometrical structure made of non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)]. Bone graft is typically used to help with osseointegration.

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

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Manufacturer

Manufacturer: Pantheon Spinal LLC

Sources (1)

FDA UDI 4d63f3f5-2b42-4890-9ae7-bef3136abefa 36 fields · synced Jun 21, 2026