A repeatable matrix process
An iPSC-derived, collagen-rich extracellular matrix process aimed at repeatable matrix production.
Research programThe biologics behind the fusion, from allograft and synthetics to the patient’s own MSCs.
Cortical fiber, DBM putty and cancellous bone in moldable, flowable and strip forms.

Bioactive glass, bioceramic and collagen matrices in putty, strip and granule form.

A focused system for recovering the patient’s own marrow-derived MSCs at the point of care.

Every graft we ship is going into someone who wants their morning back. That is the standard we hold the portfolio to.
Bioactive glass in orbital form. PURactiveOrb packs bioactive glass into engineered orbs of two sizes, about 80% glass by weight, in a moldable, non-hardening phospholipid putty. The orbs pack densely, present a large bioactive surface for cellular attachment, and leave open spaces between them for new bone to grow into.


PURbonedough is 100% human cortical bone, cut into short fibers that interlock when you hydrate them into a dough that holds together, packs where you put it and stays put under irrigation. Nothing in the jar but bone, and every lot tested for osteoinductive potential before it ships.
Accreditation and sterility assurance are where every tissue supplier starts. These are the steps beyond that, learned from decades in the field.
Donor source quality and selection judgment built case by case, not read from a spec sheet.
Allograft DBM lots are tested for osteoinductive potential before release, not sampled.
Processing designed to deliver a sterile graft without degrading the activity surgeons are relying on.
Multiple qualified tissue sources so supply does not dictate the surgeon's choice of graft.

PURactiveOrb is available with a minimally invasive delivery option: a trigger-fed instrument and cannula that place putty through a small access corridor.
PUR Biologics is a commercial-stage orthobiologics company based in Irvine, California. For thirteen years we have brought allograft, synthetic graft and MSC-recovery products to spine and orthopedic surgeons through a focused portfolio and direct relationships with the people who use it.
We work with surgeons, hospitals and surgery centers, and distribution partners across the United States.

A 510(k)-cleared HA/TCP sphere platform in a mesh format for posterolateral spine graft extension, moving through manufacturing transfer.
Granted patents and applications spanning extracellular matrix manufacturing and regenerative cell-activation technologies.
Three research directions exploring how matrices and defined chemistry can inform future biologic technologies.
Product literature, current instructions for use, ordering, or a conversation about distribution. Our team answers directly.
Twelve products across three families: allograft, synthetics and MSC recovery.
Bioactive glass in orbital form. Engineered orbs of two sizes, about 80% glass by weight, in a resorbable phospholipid carrier: moldable, non-hardening, resists irrigation, and ready through a 9 mm cannula.

Bioactive glass is among the most studied synthetic graft materials in orthopedics. Conventional putties use it as crushed, irregular particles. PURactiveOrb uses orbs: two engineered diameters, 90–180 µm and 355–500 µm, blended in a fixed ratio. The smaller orbs fill the spaces between the larger ones, so the putty packs more glass into the defect and presents a consistent, high surface area to surrounding bone, with interconnected spaces between the orbs for cells and vessels to move into.
That surface is where the material does its work. Bioactive glass forms a calcium phosphate layer at its surface after implantation, and in the orbital form every orb presents that surface for cellular attachment. The result is a putty that is about 80% bioactive glass by weight, roughly 1.5 grams of glass in every cc, bound by a natural phospholipid carrier. After placement the carrier is resorbed and the glass remains in direct contact with host bone.
In a preclinical rabbit defect model, new bone formed directly on the orb surfaces and in the spaces between them, with bone present throughout the implant area at six weeks.1
Supplied in an open-bore syringe sealed within two foil pouches, in 2.5, 5 and 10 cc volumes. No hydration step.
1 Preclinical animal study, data on file. Results in animal models do not necessarily predict clinical performance in humans.

A trigger-fed instrument and cannula place PURactiveOrb through a minimally invasive corridor in controlled increments.
PURactiveOrb Putty is indicated for bony voids or gaps that are not intrinsic to the stability of the bony structure. It is indicated as a bone void filler in the extremities and pelvis, and as a bone graft extender in the posterolateral spine.
For posterolateral fusion, PURactiveOrb Putty must be mixed with autograft in a 1:1 ratio.
This summary does not replace the complete instructions for use, including contraindications, warnings, precautions and directions.
Do not add fluid directly to the putty, including blood or saline. This may negatively affect handling and cohesiveness. Refer to the current IFU for preparation and use.
The product does not possess sufficient mechanical strength to solely support defect reduction. Appropriate stabilization is required. The product is for single-patient, single use only.
100% human cortical bone in a dough that holds together, packs where you put it and stays put under irrigation. Nothing in the jar but bone.

PURbonedough is made from 100% human cortical bone, processed into short fibers. There is no extrinsic carrier: no collagen, no gelatin, no synthetic binder. When the fibers are hydrated they interlock into a cohesive dough, so the graft handles like a putty while every gram of it is bone.
Supplied dry in a jar, stored at room temperature, with a five-year shelf life from the date of packaging.
PURbonedough is hydrated in the field with the fluid the surgeon chooses: saline, whole blood, bone marrow aspirate or platelet-rich plasma, at the physician’s discretion. The fibers take up the fluid and bind into a dough that can be shaped, packed and held in place.




Demineralized bone is only as good as the lot in your hand. Every lot of PURbonedough is tested for osteoinductive potential by an independent laboratory after sterilization and before release. Not sampled. Not inferred from a sister lot. Tested.

PURbonedough is a human tissue allograft intended for homologous use in the repair, replacement or reconstruction of surgically created or traumatic skeletal defects.
This summary does not replace the complete instructions for use, including contraindications, warnings, precautions and directions. Human tissue is regulated under 21 CFR Part 1271.
Hydrate per the instructions for use with the fluid selected by the physician. Do not re-sterilize. Single patient, single use.
Store at ambient temperature, 15–30 °C (59–86 °F). Do not use after the expiration date on the label.
Distinctive materials, protected technologies and a research program built around regenerative medicine.
A synthetic graft platform of porous HA/TCP spheres contained in a mesh format, developed for posterolateral spine graft extension. The platform is 510(k)-cleared; manufacturing transfer and shelf-life work are the next milestones on the path to commercial release.
This platform is distinct from PURactiveOrb Putty, our bioactive glass product.
PUR's intellectual-property portfolio spans extracellular matrix manufacturing and regenerative cell-activation technologies, with patent work extending into bone and cartilage programs. These technologies form the foundation for a research pipeline that reaches beyond today's commercial catalog.
An iPSC-derived, collagen-rich extracellular matrix process aimed at repeatable matrix production.
Research programPatent work spanning cartilage regeneration, alongside PUR's broader matrix and bone-focused programs.
Patent & research focusA defined molecular composition intended to activate bone-marrow-derived immune cells, with bone regeneration as an initial application.
Research programResearch programs describe development objectives, not established clinical outcomes or commercially available treatments. The sphere platform's clearance does not apply to the ECM, cartilage or immune-activation programs.