Vital™

FDA UDI

Class I (US FDA UDI)

by Biomet Spine Llc

Identity

Trade Name: Vital™ FDA UDI
Generic Name: Surgical instrument handle, torque-limiting FDA UDI
Model / Reference: 850M0050 FDA UDI

Identifiers

Catalog Number: 850M0050 FDA UDI
Primary DI / UDI-DI: 00887868310072 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Surgical instrument handle, 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

FDA UDI

Single Use

FDA UDI

Implantable

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

Yes

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

Category: Surgical instrument handle, torque-limiting

Vital™ by Biomet Spine Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Surgical instrument handle, torque-limiting.

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InCore MPJ — Medartis Inc. · Class I
KONG-TL VBR System, Torque Limiter with Coupling, 1/4'' Coupling, 1 Nm — Icotec · 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 I	Pending data

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Manufacturer

Manufacturer: Biomet Spine Llc

Sources (1)

FDA UDI 2c48279c-86f3-4ff4-bced-7ff1864aa7d3 35 fields · synced Jun 8, 2026