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Vyrsa V1

FDA UDI

Class I (US FDA UDI)

by Vyrsa Technologies

Identity

Trade Name
VYRSA V1 FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
VI Extended Inserter Assembly FDA UDI
Model / Reference
VYV1-103-321 FDA UDI
Description
VI Extended Inserter Assembly FDA UDI

Identifiers

Primary DI / UDI-DI
G418VYV11033210 FDA UDI
510(k) Number
K203503 FDA UDI
K233972 FDA UDI
FDA Product Code
LXH FDA UDI
OUR FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
888.3040 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: Orthopaedic inorganic implant inserter/extractor, reusable

Vyrsa V1 by Vyrsa Technologies — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, reusable.

Cleared under the same submission

K203503 also covers:

K233972 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vyrsa Technologies

Sources (1)

  • FDA UDI 5dbe2612-be1e-46c8-ba3e-aa07facbd468 34 fields · synced Jun 8, 2026