Florida Healthcare Providers · Senate Bill 1768 · For Investigational Use Per FL Statute
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REVIVE AESTHETICS
ZEO Distribution Confidential · 2026
Day Zero. Peak Vitality.

Upgrade
your stem cells.

DayZero™ biologics are collected within hours of delivery — when cells and signaling vesicles are at peak vitality. FDA-registered facility. cGMP-compliant manufacturing. Per-lot certificate of analysis.

0
Day Zero Collection
Hours from Delivery
4
Product Lines
UC · WJ · Membrane · PPX
cGMP
FDA-Registered
Manufacturing
COA
Per-Lot Certificate
of Analysis
DayZero umbilical cord stem cells
Day Zero · Peak Vitality DayZero™ Stem Cells FDA-Registered · cGMP Ethically Sourced Per-Lot COA FL Senate Bill 1768 Florida Physicians Only Day Zero · Peak Vitality DayZero™ Stem Cells FDA-Registered · cGMP Ethically Sourced Per-Lot COA FL Senate Bill 1768 Florida Physicians Only
The Full Lineup

Four product lines.
One manufacturing standard.

DayZero™ stem cells, Wharton's Jelly Matrix, Amniotic Membrane Patches, and Patient Pure X™ autologous EVs — every lot processed in an FDA-registered, cGMP-compliant facility and ships with a certificate of analysis.

DayZero Stem Cells
01 · DayZero™
Umbilical Cord
Stem Cells
Day Zero Collection · Cryopreserved
Umbilical cord–derived stem cells with high live-cell counts, collected within hours of delivery and processed in cGMP-compliant facilities.
Available Formats
10M Vial 20M Vial 100M IV Bag 120M IV Bag 150M IV Bag
◆Orthopedics  ◆Pain Management  ◆Wound Care
Wharton's Jelly Matrix
02 · DayZero™
Wharton's
Jelly Matrix
Gelatinous Scaffold · EV-Rich
Natural collagen and hyaluronic-rich gelatinous matrix combined with a dense extracellular vesicle payload. Single-use sterile preparations.
Available Formats
50B EV 100B EV 200B EV
◆Orthopedics  ◆Wound Care  ◆Pain Management
Amniotic Membrane Patches
03 · DayZero™
Amniotic
Membrane Patches
Optical Discs · Custom Sheets
Extracellular membrane sheets retain endogenous growth factors and an intact collagen network. An easy-to-handle biological dressing for surgical closure and chronic wounds.
Available Formats
12 mm Optical Disc Custom Sheet Sizes
◆Surgical Closure  ◆Chronic Wound Care
Patient Pure X autologous EVs
04 · Patient Pure X™
PPX™
Autologous EVs
Patient-Derived · Chair-Side
Begins with the patient's own platelets, collected chair-side and processed in cGMP facilities. Removes RBCs and leukocytes; concentrates platelet-derived EV fraction with growth factors and micro-RNA.
Available Formats
100B EV 200B EV 400B EV
◆Orthopedics  ◆Pain Management  ◆Wound Care
The Day Zero Standard

Why day zero matters.

The window between birth and processing is everything. ZEO's DayZero™ protocol compresses that window — and locks in cell viability through cryopreservation.

i · Collection
Within hours of birth.
Tissue is collected from screened, consented donors within hours of delivery — when cells and signaling vesicles are at peak vitality.
ii · Processing
FDA-registered. cGMP-compliant.
Material is processed in an FDA-registered, cGMP-compliant facility with documented chain of custody and standardized protocols across every lot.
iii · Cryopreservation
Locked in. Released with COA.
Each lot is cryopreserved to preserve potency and ships with a certificate of analysis confirming sterility, identity, and post-thaw viability.
Why ZEO

Four standards. No exceptions.

Most distributors sell the box. ZEO sells the documentation behind it. Every vial. Every lot. Every time.

i · Day Zero Sourcing

Hours, not days.

Tissue is collected within hours of delivery, when cells and signaling vesicles are at peak vitality. Late collection means degraded material. ZEO doesn't ship that.

ii · Ethical Sourcing

Screened. Consented.

All donor tissue comes from screened, consented donors via established perinatal partner programs. No gray-market material. No undocumented sourcing. Ever.

iii · FDA + cGMP Manufacturing

Registered facility.

Every product is manufactured in an FDA-registered, cGMP-compliant facility with documented protocols, environmental controls, and chain-of-custody from collection through release.

iv · Per-Lot Documentation

Certificate of analysis.

Every lot ships with a certificate of analysis confirming sterility, identity, and post-thaw viability. Physicians know exactly what they're injecting before they open the vial.

Authorized Indications

Three categories. Florida physicians only.

Per Florida Senate Bill 1768 (effective July 1, 2025), stem cell therapies as defined in the statute are available to FL physicians for the following therapeutic indications.

Indication 01
Orthopedics
Joint, tendon, and ligament applications across the spine and extremities. Compatible with standard orthopedic injection workflows.
Indication 02
Pain
Management
Chronic pain protocols including epidural and peri-articular applications. IV bag formats support systemic protocols.
Indication 03
Wound Care
Surgical closure and chronic wound dressing applications using amniotic membrane patches and EV-rich Wharton's Jelly Matrix.
Practice Standards

Documented. Traceable. Defensible.

Regenerative medicine lives or dies on documentation. Here's the paper trail that comes standard with every ZEO order.

Quality assurance, built into every lot.
ZEO products ship with per-lot certificates of analysis confirming sterility, identity, and viability — alongside chain-of-custody documentation tracing material from screened donor to your office. The infrastructure that protects your license travels with the product.
FDA
Registered Facility
Documented Protocols
cGMP
Compliant Manufacturing
Environmental Controls
COA
Per-Lot Documentation
Sterility · Identity · Viability
SB 1768
FL Statute Compliant
Authorized Indications
— Revive Aesthetics · ZEO Distribution —

Upgrade your stem cells.

Day Zero · Peak Vitality · Documented

Get In Touch

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Florida Senate Bill 1768 became law on July 1, 2025 and amended FS §458.3245 and FS §459.0127, making stem cell therapies as defined in the statute available for the following therapeutic indications: orthopedics, wound care, and pain management. Material on this page is intended for general informational and educational purposes only and is not intended to provide medical advice, diagnosis, or treatment recommendations. ZEO ScientifiX does not make any medical claims regarding any of these products. ZEO ScientifiX does not offer medical services to the public and does not endorse or guarantee any third-party products or services referenced. Content may reference investigational biologics or devices not approved by the FDA. This material is intended for Florida physicians only. Any mention of product usage is for therapeutic use only in the states of Florida and Utah. Subject to change without notice. Revive Aesthetics is an authorized distribution partner.