FDA.reportPublic FDA data

TAMPER

Primary DI
00888118027832
Brand
TAMPER
Company
KLS-Martin L.P.
Model
23-198-08-07
Published
2018-09-26
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
false

Contact Domains#

Product Codes#

Code, Name table
CodeName
HXGTAMP

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HXGTampOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00888118027832PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00888118027832008881180278328881180278320888118027832

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic implant impactorA metal and/or plastic hand-held manual surgical instrument designed to position an implant into the body. Its mode of application is by transmission of an impact force to drive the implant into its final position in the body. The proximal end is a handle usually designed to absorb the impact from a surgical hammer or mallet. The distal end is usually shaped to conform to the implant shape, which could be flat or anatomically curved, or shaped like a chisel handle to facilitate the positioning. This is a reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(904)641-7746KLS-UDI-Info@klsmartin.com

Regulatory Flags#

DUNS number
826499238
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00888118131782LEVEL ONE EXTREMITY26-066-60-092026-05-25
00888118131799LEVEL ONE EXTREMITY26-066-70-092026-05-25
00888118144928LEVEL ONE EXTREMITY26-950-40-072026-05-25
00888118145284PURE PECTUS24-070-60-092026-05-25
00888118145291PURE PECTUS24-070-62-092026-05-25
00888118150240PURE PECTUSCTM-241-100-012026-05-25
00888118150257PURE PECTUSCTM-241-101-012026-05-25
00888118150264PURE PECTUSCTM-241-200-012026-05-25
00888118150448IXOSCTM-263-100-012026-05-25
00888118150455IXOSCTM-263-101-012026-05-25
00888118150462IXOSCTM-263-202-012026-05-25
00888118150479IXOSCTM-263-202-022026-05-25
00888118150486IXOSCTM-263-202-032026-05-25
00888118150493IXOSCTM-263-202-042026-05-25
00888118150646IPS60-011-42-09-LP2026-05-25
00888118153029L1 STERNALCTM-242-302-012026-05-25
00888118153050IXOSCTM-263-203-012026-05-25
00888118153067IXOSCTM-263-203-022026-05-25
00888118153074IXOSCTM-263-203-032026-05-25
00888118153081IXOSCTM-263-203-042026-05-25

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00190776416423MillenniumAvalign Technologies, Inc.HXG2026-02-16
00190776416430MillenniumAvalign Technologies, Inc.HXG2026-02-16
00190376538990Intervertebral Disc Preparation InstrumentsALPHATEC SPINE, INC.HXG2026-02-10
00190376694351IdentiTiALPHATEC SPINE, INC.HXG2026-02-10
00190376694368Intervertebral Disc Preparation InstrumentsALPHATEC SPINE, INC.HXG2026-02-10
00190376700700IdentiTiALPHATEC SPINE, INC.HXG2026-02-10
00190376700717IdentiTiALPHATEC SPINE, INC.HXG2026-02-10
00810112598902TriLeap Lower Extremity Anatomic Plating SystemCROSSROADS EXTREMITY SYSTEMSHXG2026-02-10
00190776415723MillenniumAvalign Technologies, Inc.HXG2026-02-04
04026575341153Endo-Model Knee Fusion Nail SK InstrumentsWALDEMAR LINK GmbH & Co. KGHXG2026-02-02
00840180543429General InstrumentsALPHATEC SPINE, INC.HXG2025-12-31
00840180543597General InstrumentsALPHATEC SPINE, INC.HXG2025-12-31
00840180543757General InstrumentsALPHATEC SPINE, INC.HXG2025-12-31
03662663155625Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-29
03662663156707Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-29
10889981285999FacetSeaspine Orthopedics CorporationHXG2025-12-19
03662663242233Alta ACDF SystemHighridge Medical, LLCHXG2025-12-18
03662663242240Alta ACDF SystemHighridge Medical, LLCHXG2025-12-18
03662663160674Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-16
03662663160681Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-16
03662663160698Zyston Interbody Spacer SystemHighridge Medical, LLCHXG2025-12-16
03662663246620Alta ACDF SystemHighridge Medical, LLCHXG2025-12-16
03662663254113Alta ACDF SystemHighridge Medical, LLCHXG2025-12-16
03662663254120Alta ACDF SystemHighridge Medical, LLCHXG2025-12-16
00190376662176IdentiTi IIALPHATEC SPINE, INC.HXG2025-12-08
00199150041930Medtronic Reusable InstrumentsMEDTRONIC SOFAMOR DANEK, INC.HXG2025-11-20
03662663070942TMT InstrumentsHighridge Medical, LLCHXG2025-11-16
03662663071581TMT InstrumentsHighridge Medical, LLCHXG2025-11-16
00888480363101C-THRU Anterior Spinal Spacer SystemHighridge Medical, LLCHXG2025-11-14
00888480637370Breckenridge ACDF SystemHighridge Medical, LLCHXG2025-11-14