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Panta® 2

FDA UDI

Class I (US FDA UDI)

by Ascension Orthopedics, Inc.

Identity

Trade Name
Panta® 2 FDA UDI
Generic Name
Surgical instrument handle, non-torque-limiting FDA UDI
Device Name
Arthrodesis Nail System T-Handle with AO Quick Connect FDA UDI
Model / Reference
HTM0111-S01 FDA UDI
Description
Arthrodesis Nail System T-Handle with AO Quick Connect FDA UDI

Identifiers

Catalog Number
HTM-0111-S01 FDA UDI
Primary DI / UDI-DI
10381780505778 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical instrument handle, non-torque-limiting FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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: Surgical instrument handle, non-torque-limiting

Panta® 2 by Ascension Orthopedics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument handle, non-torque-limiting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ascension Orthopedics, Inc.

Sources (1)

  • FDA UDI b1c67d11-dd7d-4aa0-8e32-1c99e9e5cb99 37 fields · synced Jun 6, 2026