← Back to catalogue

Mbcp

FDA UDI

Class II (US FDA UDI)

by Biomatlante

Identity

Trade Name
MBCP FDA UDI
Generic Name
Bone matrix implant, synthetic, non-antimicrobial FDA UDI
Device Name
Synthetic Bone Substitute Granules FDA UDI
Model / Reference
0802G05 FDA UDI
Description
Synthetic Bone Substitute Granules FDA UDI

Identifiers

Catalog Number
0802G05 FDA UDI
Primary DI / UDI-DI
03700501800662 FDA UDI
510(k) Number
K051774 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Bone matrix implant, synthetic, non-antimicrobial FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3045 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Dimensions & Sizes

Size
Total Volume — 5 Milliliter FDA UDI

Category: Bone matrix implant, synthetic, non-antimicrobial

Mbcp by Biomatlante — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone matrix implant, synthetic, non-antimicrobial.

Cleared under the same submission

K051774 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Biomatlante

Sources (1)

  • FDA UDI 4e73c79d-13f5-4084-a2a1-b30c0442026e 37 fields · synced May 30, 2026