ThriveSynth™ Calcium Putty is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, ThriveSynth™ Calcium Putty resorbs and is later replaced by natural bone.…
ThriveSynth™ Calcium Putty is a bio-engineered mixture of calcium-based inorganic compounds. After it is implanted, ThriveSynth™ Calcium Putty resorbs and is later replaced by natural bone. ThriveSynth™ Calcium Putty is a natural choice for sparing patients the trauma of autograft harvesting. It also provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission. ThriveSynth™ Calcium Putty is an osteoconductive putty that is intended to be used to fill voids and gaps that are not intrinsic to the stability of the bone structure. These gaps or voids may be located in the extremities, spine, pelvis, or cranium. The putty may be shaped and pressed into the void by hand or inserted into a syringe and injected into the surgical site. The paste set in situ or ex situ provides a void filler that can augment hardware to support bone fragments during the surgical procedure. The set putty acts as a temporary support medium and is not intended to provide structural support during the healing process. The implant is radio-opaque. It is biocompatible and resorbs in the body as bone in-growth occurs.
Who Else Makes It
Concentrated in Shanghai (1), Beijing (1).
Record
Regulatory record for ThriveSynth™ Calcium Putty | Listed by | Berkeley Advanced Biomaterials, United States |
| FDA product code | MQV |
| Device type | Filler, Bone Void, Calcium Compound |
| Device class | Class 2 |
| Regulation | 21 CFR 888.3045 |
| Establishment | Manufacturer |
| 510(k) | K022622 |
| Record published | 2026-05-19 |
Specifications
Specifications | MRI safety | Labeling does not contain MRI Safety Information |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Supplied as a kit | Yes |
| Label carries | lot or batch number, expiry date, serial number |
Recalls
1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.