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Regenalase

FDA UDI

Class II (US FDA UDI)

by IPG Medical Corporation

Identity

Trade Name
Regenalase FDA UDI
Generic Name
Musculoskeletal/physical therapy laser, professional FDA UDI
Device Name
Universal Stage One Handpiece FDA UDI
Model / Reference
MD2300F-001754 FDA UDI
Description
Universal Stage One Handpiece FDA UDI

Identifiers

Primary DI / UDI-DI
00810071230547 FDA UDI
FDA Product Code
ILY FDA UDI
GMDN Term
Musculoskeletal/physical therapy laser, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5500 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Musculoskeletal/physical therapy laser, professional

Regenalase by IPG Medical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Musculoskeletal/physical therapy laser, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 090bc3f7-d1aa-40c1-9420-aa78c933ff66 33 fields · synced Jun 9, 2026