FDA.reportPublic FDA data

ThermiRF

Primary DI
00817771029501
Brand
ThermiRF
Company
Celling Biosciences
Model
ThermiRF Eye
Catalog number
ThermiEye
Device description
Thermi RF Radiofrequency Temp Controlled Generator - Thermi Eye
Published
2025-04-11
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K130689000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K130689000SYMPHONY RF GENERATORThermigen, Inc.2013-11-15GEI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00817771029501PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00817771029501008177710295018177710295010817771029501

GMDN Terms#

Term, Definition table
TermDefinition
Percutaneous radio-frequency ablation system generatorAn electrically-powered, noninvasive device designed to generate radio-frequency (RF) electrical current used to create heat via a percutaneously (through the skin) introduced electrode(s) in a precise location, at a controlled temperature, for focal ablation of non-cardiac tissues (e.g., non-cardiac nerves, tumours, precancerous tissue); it may be intended for coagulation however it is not intended for electrosurgical cutting. The generator connects via a delivery cable to an electrosurgical ablation probe/catheter (not included) to transmit the RF electrical current to the operative site; it might additionally be intended to heat an electrode tip (electrocautery).

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
021560394
Device count
1
DM exempt
true
Serial number
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00817771027316SpineSmith Fusionary Graft Delivery System0851-00300851-00302016-12-29
00817771027323SpineSmith Fusionary Graft Delivery System0851-00610851-00612016-12-29
00817771027354SpineSmith Fusionary Graft Delivery System0851-10600851-10602016-12-28
00817771027361SpineSmith Fusionary Graft Delivery System0851-10700851-10702016-12-28
00817771027378SpineSmith Fusionary Graft Delivery System0851-30600851-30602016-12-29
00817771027385SpineSmith Fusionary Graft Delivery System0852-00010852-00012016-12-29
00817771027392SpineSmith Fusionary Graft Delivery System0852-01200852-01202016-12-29
00817771029761Solum FlowSolum Flow - 10cc1206-01002025-08-05
00817771027637SpineSmith IN:C2 Spinal Fixation System1100-0002-PL1100-0002-PL2018-02-14
00817771029815SpineSmith IN:C2 Spinal Fixation System1110-0001-PL1110-0001-PL2018-02-14
00817771029822SpineSmith IN:C2 Spinal Fixation System1110-0002-PL1110-0002-PL2018-02-14
00817771027439ART BMC System Centrifuge0882-00010882-00012025-04-11
00817771027460ART BMC System Centrifuge0882-00040882-00042025-04-11
00817771027484ART BMC System Centrifuge0882-00200882-00202025-04-11
00817771028788Celling ART BMC Plus 0866-00020866-00022025-04-11
00817771028795Celling ART BMC 0886-00010886-00012025-04-11
00817771028825Celling ART PRP 2-Step 60 Kit1651-00041651-00042025-04-11
00817771028849Celling Cardio Application Kit0851-00030851-00032025-04-11
00817771028856Celling ART PRP 2-Step 120 Kit1651-00051651-00052025-04-11
00817771028870Celling ART PRP 2-Step Mini Kit1651-00021651-00022025-04-11

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