FDA.reportPublic FDA data

StimTrial Patient Kit

Primary DI
00816986020570
Brand
StimTrial Patient Kit
Company
BIOVENTUS LLC
Model
TS-6000
Published
2025-09-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Unsafe
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GZFStimulator, Peripheral Nerve, Implanted (Pain Relief)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GZFStimulator, Peripheral Nerve, Implanted (Pain Relief)Neurology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K243782000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K243782000StimTrial Neuromodulation SystemBioventus, LLC2025-07-16GZF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00816986020570PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00816986020570008169860205708169860205700816986020570

GMDN Terms#

Term, Definition table
TermDefinition
Spinal cord/peripheral nerve implantable analgesic electrical stimulation system pulse generator, extracorporealAn electrically-powered, external (noninvasive) component of a spinal cord/peripheral nerve implantable analgesic electrical stimulation system intended to generate electrical impulses, for wireless (transcutaneous) transmission, to an implantable lead (situated adjacent to the epidural space and/or a peripheral nerve), to relieve acute and/or chronic intractable pain (analgesia); the implantable lead is not included. It is designed for continuous therapy (i.e., not a trial therapy device). The device is programmed, controlled, and charged by external devices which may be included with the device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Humidity10 Percent (%) Relative Humidity90 Percent (%) Relative Humidity
Storage Environment Humidity50 KiloPascal106 KiloPascal
Storage Environment Temperature-29 Degrees Celsius60 Degrees Celsius

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
888-453-2136CustomerServiceUSA@bioventusglobal.com

Regulatory Flags#

DUNS number
078450878
Device count
1
Kit
true
Lot or batch
true
Serial number
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
M937710346601EXOGEN Metatarsal Strap710346602021-12-17
M937710344001EXOGEN® Ultrasound Bone Healing System71034400710344002017-01-12
M937710346001EXOGEN® Ultrasound Bone Healing System71034600710346002017-01-12
00816986020549TalisMann Implant KitTM-10002025-09-01
00816986020556StimTrial Surgical KitTS-10002025-09-01
00816986020587StimTrial Stimulator KitTS-50002025-09-01
00816986020617Bioventus User KitPNS-50002025-09-01
00816986020624Bioventus Clinician KitPNS-10002025-09-01
10389130444418SUPARTZ FX sodium hyaluronate715644442023-09-28
00816986020525Osteoamp Flowable Access CannulaOFAC-COFAC-C2024-11-21
00816986020037INTERFACEIFBG100IFBG1002019-05-06
00816986020488SIGNAFUSE Bioactive Bone Graft25X25X8 MM, 5 CCSGFS-0052020-07-30
00816986020495SIGNAFUSE Bioactive Bone Graft50X25X8 MM, 10 CCSGFS-0102020-07-30
00816986020501SIGNAFUSE Bioactive Bone Graft100X25X8 MM, 20 CCSGFS-0202020-07-30
00816986020518SIGNAFUSE Bioactive Bone Graft200X25X8 MM, 40 CCSGFS-0402020-07-30
00816986020006SIGNAFUSE15gSGF-1502019-02-22
00816986020013SIGNAFUSE7.5gSGF-0752019-02-22
00816986020020SIGNAFUSE3.75gSGF-0372019-02-22
00816986020082OSTEOFUSE3.75gOF0012019-02-22
00816986020099OSTEOFUSE7.5gOF0022019-02-22

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00812537030234Therapy DiscNALU MEDICAL, INC.GZF2026-01-19
00812537032399Therapy DiscNALU MEDICAL, INC.GZF2026-01-19
00812537035802Therapy Disc, Reduced WarrantyNALU MEDICAL, INC.GZF2026-01-19
00812537035925Nalu Medical, Inc.NALU MEDICAL, INC.GZF2024-01-02
00812537036021Nalu Medical, Inc.NALU MEDICAL, INC.GZF2024-01-02
00812537032917Nalu Medical, Inc.NALU MEDICAL, INC.GZF2022-09-30
00812537034317Nalu Medical, Inc.NALU MEDICAL, INC.GZF2022-09-30
00812537034355Nalu Medical, Inc.NALU MEDICAL, INC.GZF2022-09-30
00812537030630Nalu Medical, Inc.NALU MEDICAL, INC.GZF2021-12-10
00812537031910Nalu Medical, Inc.NALU MEDICAL, INC.GZF2021-12-10
00812537032986Nalu Medical, Inc.NALU MEDICAL, INC.GZF2021-12-10
00812537035567Nalu Medical, Inc.NALU MEDICAL, INC.GZF2021-12-10
00812537036076Nalu Medical, Inc.NALU MEDICAL, INC.GZF2021-12-10
00812537036083Nalu Medical, Inc.NALU MEDICAL, INC.GZF2021-12-10
00812537036090Nalu Medical, Inc.NALU MEDICAL, INC.GZF2021-12-10
00812537033822Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-10-12
00812537033303Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-08-20
00812537035734Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-06-24
00812537035741Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-06-24
00812537035758Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-06-24
00812537030050Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030067Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030074Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030098Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030104Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030111Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030128Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030135Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030142Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21
00812537030166Nalu Medical, Inc.NALU MEDICAL, INC.GZF2020-04-21