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Epiphany

FDA UDI

Class II (US FDA UDI)

by Pantheon Spinal LLC

Identity

Trade Name
Epiphany FDA UDI
Generic Name
Implant handling forceps, scissors-like FDA UDI
Device Name
Bayonet Bipolor Forcep FDA UDI
Model / Reference
1 FDA UDI
Description
Bayonet Bipolor Forcep FDA UDI

Identifiers

Catalog Number
1019-0000 FDA UDI
Primary DI / UDI-DI
B528101900000 FDA UDI
510(k) Number
K113781 FDA UDI
FDA Product Code
MAX FDA UDI
GMDN Term
Implant handling forceps, scissors-like 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

Category: Implant handling forceps, scissors-like

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

Similar devices

Also classified as Implant handling forceps, scissors-like.

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 bd447c1f-1d89-410f-8340-50746b1642fd 36 fields · synced May 30, 2026