FDA.reportPublic FDA data

TruForm

Primary DI
08809204338764
Brand
TruForm
Company
Hans Biomed Corp.
Model
FG050DEMO
Device description
5.0cc(DEMONSTRATION)
Published
2017-07-18
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
MBPFiller, Bone Void, Osteoinduction (W/O Human Growth Factor)
MQVFiller, Bone Void, Calcium Compound
NUNBone Grafting Material, Human Source

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MBPFiller, Bone Void, Osteoinduction (W/O Human Growth Factor)Orthopedic2
MQVFiller, Bone Void, Calcium CompoundOrthopedic2
NUNBone Grafting Material, Human SourceDental2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08809204338764PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08809204338764088092043387648809204338764

GMDN Terms#

Term, Definition table
TermDefinition
Human-derived demineralized bone matrix implantAn implantable device made primarily of human demineralized bone matrix (DBM) (acid extraction of allogeneic bone resulting in loss of most of the mineralized component but retention of proteins) intended to fill bony voids or gaps caused by trauma or surgery, including use in the maxillofacial and/or mandibular bone. The device is bioabsorbable, osteoconductive, and has demonstrated at least potential osteoinductivity for the stimulation of new bone growth. The DBM may be combined with various carrier compounds (e.g., gelatin, hydrogel, starch) or other materials. It is available in the form of powder, crushed granules, putty, chips, or a gel that can be injected through a syringe.

Regulatory Flags#

DUNS number
689512625
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
true
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08809204338498ExponentEXP002017-03-09
08809204338580TruForm+TFP003DEMO2017-07-18
08809204338597TruForm+TFP005DEMO2017-07-18
08809204338603TruForm+TFP010DEMO2017-07-18
08809204338610TruForm+TFP030DEMO2017-07-18
08809204338627TruForm+TFP050DEMO2017-07-18
08809204338634TruForm+TFP100DEMO2017-07-18
08809204338641TruForm+TFG010DEMO2017-07-18
08809204338658TruForm+TFG030DEMO2017-07-18
08809204338665TruForm+TFG050DEMO2017-07-18
08809204338672TruForm+TFG100DEMO2017-07-18
08809204338689TruFormFP003DEMO2017-07-18
08809204338696TruFormFP005DEMO2017-07-18
08809204338702TruFormFP010DEMO2017-07-18
08809204338719TruFormFP030DEMO2017-07-18
08809204338726TruFormFP050DEMO2017-07-18
08809204338733TruFormFP0100DEMO2017-07-18
08809204338740TruFormFG010DEMO2017-07-18
08809204338757TruFormFG030DEMO2017-07-18
08809204338771TruFormFG100DEMO2017-07-18

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00199284455788BonVie+ELUTE , INC.MQV2025-08-13
00191083045092RegenaVate™ Formable DBM, 1cm x 4cm x 0.5cm, 2ccRti Surgical, Inc.NUN2024-05-27
00191083045108RegenaVate™ Formable DBM RT, 1ccRti Surgical, Inc.NUN2024-05-27
00191083045078RegenaVate™ Formable DBM, 1cm x 1cm x 0.5cm, 0.5ccRti Surgical, Inc.NUN2024-05-27
00191083045085RegenaVate™ Formable DBM, 1cm x 2cm x 0.5cm, 1ccRti Surgical, Inc.NUN2024-05-27
00191083045115RegenaVate™ Formable DBM RT, 2ccRti Surgical, Inc.NUN2024-05-27
00085412630731ALTAPOREApatech LtdMQV2020-11-05
00085412678146ALTAPOREApatech LtdMQV2020-11-05
00085412654362ALTAPOREApatech LtdMQV2019-12-11
00085412654379ALTAPOREApatech LtdMQV2019-12-11
00085412654386ALTAPOREApatech LtdMQV2019-12-11
00085412654393ALTAPOREApatech LtdMQV2019-12-11
00613994247612PROGENIX® PUTTY and PROGENIX® PLUSMEDTRONIC SOFAMOR DANEK, INC.MBP2019-03-29
00613994247612PROGENIX® PUTTY and PROGENIX® PLUSMEDTRONIC SOFAMOR DANEK, INC.MQV2019-03-29
00613994512758MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512765MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512772MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512789MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512796MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512802MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512819MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994512826MASTERGRAFT® Mini GranulesMEDTRONIC SOFAMOR DANEK, INC.MQV2018-11-18
00613994986467MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986474MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986481MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986498MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986504MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986511MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986528MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01
00613994986535MAGNIFUSE® Bone GraftMEDTRONIC SOFAMOR DANEK, INC.MQV2015-12-01