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Musculoskeletal Transplant Foundation

USA · Edison

✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Canada — 2 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable

CNChinaNMPA

n/aThis registry lists domestic registrants only

EUEuropean UnionEUDAMED

pendingnot queried

USUnited StatesFDA openFDA

8listed device types

Class I 0Class II 8Class III 0

plus 27 registration records and 24 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

0registered devices

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

0registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

2active device licences

Class II 1Class III 1

9 including historic records

TWTaiwanTFDA

pendingnot queried

SGSingaporeHSA SMDR

pendingnot queried

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

pendingnot queried

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

pendingnot queried

RURussiaRoszdravnadzor

pendingnot queried

Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States27 registration records, 24 510(k), 0 PMA, 1 excluded

Canada2 confirmed, 0 excluded

Manufacturer names merged into this page: Musculoskeletal Transplant Foundation d/b/a/ MTF Biologics · MUSCULOSKELETAL TRANSPLANT FOUNDATION

FDA 510(k) clearances by year

12004

32005

52006

32007

32008

22009

32011

22012

12013

12019

FDA listed device types

Filler, Bone Void, Calcium Compound 1Bone Grafting Material, Human Source 1Instruments Designed For Press-Fit Osteochondral Implants 1Filler, Bone Void, Osteoinduction (W/O Human Growth Factor) 1Suture, Nonabsorbable, Synthetic, Polyethylene 1Syringe, Piston 1Methyl Methacrylate For Cranioplasty 1Lipoaspirate Washing System For Aesthetic Body Contouring 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K181633	MTF Pre-Sutured Tendon	2019-03-15
US	K121313	MTF NEW BONE VOID FILLER	2013-01-11
US	K120479	MTF FASCIA	2012-11-08
CA	71695	HEMASORB HEMOSTASIS DEVICE	Class III
CA	88918	CASCADE AUTOLOGOUS PLATELET SYSTEM	Class II

Musculoskeletal Transplant Foundation

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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