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Wizard Tcp

FDA UDI

Class II (US FDA UDI)

by S.b.m

Identity

Trade Name
WIZARD TCP FDA UDI
Generic Name
Synthetic bone graft FDA UDI
Device Name
Absorbable calcium salt bone void filler FDA UDI
Model / Reference
BIO1 Granules FDA UDI
Description
Absorbable calcium salt bone void filler FDA UDI

Identifiers

Catalog Number
W15150 FDA UDI
Primary DI / UDI-DI
03760154008372 FDA UDI
510(k) Number
K021963 FDA UDI
FDA Product Code
MQV FDA UDI
GMDN Term
Synthetic bone graft 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

Yes

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 1.5 Millimeter FDA UDI
Total Volume — 15 Milliliter FDA UDI

Category: Synthetic bone graft

Wizard Tcp by S.b.m — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Synthetic bone graft.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
S.b.m

Sources (1)

  • FDA UDI c82f8a61-4d00-41df-ba82-b14169e0fd2f 37 fields · synced May 30, 2026