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BLDG Active

FDA UDI

Class U (US FDA UDI)

by Innovacyn, Inc.

Identity

Trade Name
BLDG Active FDA UDI
Generic Name
Wound hydrogel dressing, antimicrobial FDA UDI
Model / Reference
1403 FDA UDI

Identifiers

Primary DI / UDI-DI
00818582012423 FDA UDI
510(k) Number
K150799 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Wound hydrogel dressing, antimicrobial FDA UDI

Classification

Device Class
U 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

No

FDA UDI

Over-the-Counter

Yes

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

Dimensions & Sizes

Size
Total Volume — 3 Fluid Ounce FDA UDI

Category: Wound hydrogel dressing, antimicrobial

BLDG Active by Innovacyn, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound hydrogel dressing, antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Innovacyn, Inc.

Sources (1)

  • FDA UDI 1599a698-3b29-4ef5-a619-4ba04ba45947 35 fields · synced May 31, 2026