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Ellacor

FDA UDI

Class II (US FDA UDI)

by Cytrellis Biosystems, Inc.

Identity

Trade Name
Ellacor FDA UDI
Generic Name
Cosmetic micro-needling electronic handpiece cartridge, professional FDA UDI
Device Name
Triple Needle Cartridge (2-Pack) FDA UDI
Model / Reference
EL-03N01 FDA UDI
Description
Triple Needle Cartridge (2-Pack) FDA UDI

Identifiers

Catalog Number
EL-03N01 FDA UDI
Primary DI / UDI-DI
B933EL03N011 FDA UDI
510(k) Number
K202517 FDA UDI
FDA Product Code
QAI FDA UDI
GMDN Term
Cosmetic micro-needling electronic handpiece cartridge, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cosmetic micro-needling electronic handpiece cartridge, professional

Ellacor by Cytrellis Biosystems, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cosmetic micro-needling electronic handpiece cartridge, professional.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e1d8d0ee-485f-44fe-b391-dc2246874145 36 fields · synced Jun 8, 2026