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ProgenaMatrix

FDA UDI

Class U (US FDA UDI)

by Progenacare Global, LLC

Identity

Trade Name
ProgenaMatrix FDA UDI
Generic Name
Animal-derived wound matrix dressing FDA UDI
Device Name
Human Keratin Matrix FDA UDI
Model / Reference
PM3010 FDA UDI
Description
Human Keratin Matrix FDA UDI

Identifiers

Primary DI / UDI-DI
00850017159105 FDA UDI
510(k) Number
K182010 FDA UDI
FDA Product Code
KGN FDA UDI
GMDN Term
Animal-derived wound matrix dressing FDA UDI

Classification

Device Class
U 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
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Length — 10 Centimeter FDA UDI
Width — 10 Centimeter FDA UDI

Category: Animal-derived wound matrix dressing

ProgenaMatrix by Progenacare Global, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Animal-derived wound matrix dressing.

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 3d6ba971-c332-4b92-94be-9de6a0d2bef7 37 fields · synced May 30, 2026