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Epiphany

FDA UDI

Class II (US FDA UDI)

by Pantheon Spinal LLC

Identity

Trade Name
EPIPHANY FDA UDI
Generic Name
Bone curette, reusable FDA UDI
Device Name
22MM CURVED 30 DEGREE LEFT COBB SHAFT FDA UDI
Model / Reference
1 FDA UDI
Description
22MM CURVED 30 DEGREE LEFT COBB SHAFT FDA UDI

Identifiers

Catalog Number
1001-2208 FDA UDI
Primary DI / UDI-DI
B528100122080 FDA UDI
510(k) Number
K113781 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Bone curette, reusable 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

No

FDA UDI

Implantable

No

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

Dimensions & Sizes

Size
Height — 22 Millimeter FDA UDI
Angle — 30 degree FDA UDI

Category: Bone curette, reusable

Epiphany by Pantheon Spinal LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone curette, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pantheon Spinal LLC

Sources (1)

  • FDA UDI d807db4e-1ffd-4faf-aea9-a1b1987e5501 37 fields · synced May 30, 2026