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RevoGro Putty

FDA UDI

Class II (US FDA UDI)

by Osteonovus, Inc.

Identity

Trade Name
RevoGro Putty FDA UDI
Generic Name
Bone matrix implant, synthetic, non-antimicrobial FDA UDI
Device Name
RevoGro Putty is intended to be hydrated with ultrapure water and gently packed into bony voids or gaps of the skeletal system. FDA UDI
Model / Reference
RGC05X FDA UDI
Description
RevoGro Putty is intended to be hydrated with ultrapure water and gently packed into bony voids or gaps of the skeletal system. FDA UDI

Identifiers

Primary DI / UDI-DI
00850063977036 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone matrix implant, synthetic, non-antimicrobial

RevoGro Putty by Osteonovus, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Osteonovus, Inc.

Sources (1)

  • FDA UDI d7fed851-d781-4932-b890-96322bfb4698 35 fields · synced May 29, 2026