FDA.reportPublic FDA data

Tecomet

Primary DI
00818069018887
Brand
Tecomet
Company
TECOMET INC.
Model
RB301000
Device description
Rod Bender, In-Situ 6mm Set Left & Right
Published
2020-10-08
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
HXWBender

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HXWBenderOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00818069018887PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00818069018887008180690188878180690188870818069018887

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
078749695
Device count
1
DM exempt
true
Premarket exempt
true
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00841435109506Tecomet9399995182026-10-29
00841435122925TecometPA0172026-08-07
00841435123717Tecomet464872026-07-30
00841435123724Tecomet464882026-07-30
00841435123731Tecomet464902026-07-30
00841435123557Tecomet463592025-02-07
00841435123564Tecomet463612025-02-07
00841435123571Tecomet463632025-02-07
00841435121355Tecomet2399-16-0002023-07-21
00818069019228TecometSR354002-A2020-10-08
00841435121621Tecomet2788-12-0002023-07-20
00841435119062Tecomet466322026-06-08
00818069019631TecometTR123000-A2020-10-09
00818069019655TecometTR123000-J2020-10-09
00818069019662TecometTR123000-Q2020-10-09
00818069019679TecometTR123000-Z2020-10-09
00818069019839TecometTR311000-J2020-10-09
00818069019969TecometTR415000-BN2020-10-09
00818069019976TecometTR415000-J2020-10-09
00818069015299TecometSR111000-A2020-10-08

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10887587078496NASynthes GmbHHXW2026-08-26
00840536822871Response SpineORTHOPEDIATRICS CORP.HXW2026-08-21
00840536822888Response SpineORTHOPEDIATRICS CORP.HXW2026-08-21
00840536822895Response SpineORTHOPEDIATRICS CORP.HXW2026-08-21
00840536822901Response SpineORTHOPEDIATRICS CORP.HXW2026-08-21
10705034579627N/AMedos International SàrlHXW2026-08-14
10705034579634N/AMedos International SàrlHXW2026-08-14
00840606191654Overwatch PCFSPINAL ELEMENTS, INC.HXW2026-07-31
00840606191661Overwatch PCFSPINAL ELEMENTS, INC.HXW2026-07-31
00840606191760Overwatch PCFSPINAL ELEMENTS, INC.HXW2026-07-31
B8034709150ORTHOMEDORTHO-MED, INC.HXW2026-07-14
B8034709160ORTHOMEDORTHO-MED, INC.HXW2026-07-14
B8034709170ORTHOMEDORTHO-MED, INC.HXW2026-07-14
B8034709180ORTHOMEDORTHO-MED, INC.HXW2026-07-14
B8034709190ORTHOMEDORTHO-MED, INC.HXW2026-07-14
008401944958133P Small-Mini Frag SystemORTHOPEDIATRICS CORP.HXW2026-06-10
008401944958203P Small-Mini Frag SystemORTHOPEDIATRICS CORP.HXW2026-06-10
008401944958373P Small-Mini Frag SystemORTHOPEDIATRICS CORP.HXW2026-06-10
008401944958443P Small-Mini Frag SystemORTHOPEDIATRICS CORP.HXW2026-06-10
008401944958513P Small-Mini Frag SystemORTHOPEDIATRICS CORP.HXW2026-06-10
08800089476886Surgical InstrumentJeil Medical CorporationHXW2026-04-09
08800089476893Surgical InstrumentJeil Medical CorporationHXW2026-04-09
07640332475553CURE 2.0 ACPSpineArt SAHXW2025-11-12
07640375234834PERLA ® TLSpineArt SAHXW2025-11-10
07640375234841PERLA ® TLSpineArt SAHXW2025-11-10
07640375234858PERLA ® TLSpineArt SAHXW2025-11-10
07640375234865PERLA ® TLSpineArt SAHXW2025-11-10
00190446898795Arsenal FootTrilliant Surgical, LLCHXW2025-07-01
08809695601781GSS™ and AnyPlus®GS Medical Co., Ltd.HXW2025-03-17
08809695630187GSS™ and AnyPlus®GS Medical Co., Ltd.HXW2025-03-17