FDA.reportPublic FDA data

Slim-Fit Elevator

Primary DI
00840199530120
Brand
Slim-Fit Elevator
Company
KOROS U.S.A., INC.
Model
7571-38
Catalog number
7571-38
Device description
Slim-Fit Periosteal Elevator 17.5mm Tip, 9" Handle, 5" Shaft, 14" Total Length
Published
2024-01-31
Public version status
New
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
HTEElevator

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HTEElevatorGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840199530120Direct MarkingGS10
10840199530127PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840199530120008401995301208401995301200840199530120
1084019953012710840199530127

GMDN Terms#

Term, Definition table
TermDefinition
Bone file/rasp, manual, reusableA hand-held manual surgical instrument with a surface(s) of coarse and/or fine grooves or teeth designed to scrape and smooth the surface of bone during a surgical procedure. The device is typically a one-piece instrument with grooves/teeth along all or part of its working end(s). It is available in a variety of sizes and working end designs, including straight and curved ends and often double-ended with a central handle. It is not dedicated for use at a specific anatomy (e.g., sinus, ear) and it is made of metal [e.g., stainless steel, titanium (Ti)]. This is a reusable device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store in dry place at room temperature

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
1-805-529-0825customerservice@korosUSA.com

Regulatory Flags#

DUNS number
007928633
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
true
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
00840199528837Comfort Plus Chisel7540-067540-062025-01-31
00840199507726Separator7230-107230-102024-12-31
00840199507733Separator7230-157230-152024-12-31
00840199507740Elevator7230-187230-182024-12-31
00840199507757Elevator7230-207230-202024-12-31
00840199507764Elevator7230-257230-252024-12-31
00840199507771Elevator7230-307230-302024-12-31
00840199507788Elevator7230-357230-352024-12-31
00840199507795Elevator7230-407230-402024-12-31
00840199507801Elevator7230-427230-422024-12-31
00840199507818Elevator7230-437230-432024-12-31
00840199507870Elevator7230-607230-602024-12-31
00840199507900Hook7232-057232-052024-12-31
00840199507917Hook7232-107232-102024-12-31
00840199507924Hook7232-157232-152024-12-31
00840199507962Elevator7232-287232-282024-12-31
00840199507979Vein Retractor7232-307232-302024-12-31
00840199507986Vein Retractor7232-357232-352024-12-31
00840199507993Vein Retractor7232-407232-402024-12-31
00840199511426Chisel7315-217315-212024-12-31

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
10885862659507N/AExactech, Inc.HTE2026-03-19
10885862661364NovationExactech, Inc.HTE2026-03-19
M93072015102SF20Life InstrumentsLife Instrument CorporationHTE2026-03-06
M93072015342S20Life InstrumentsLife Instrument CorporationHTE2026-03-06
M93072015342SF20Life InstrumentsLife Instrument CorporationHTE2026-03-06
00840277133373Innomed, Inc.INNOMED, INC.HTE2026-02-26
00840277133380Innomed, Inc.INNOMED, INC.HTE2026-02-26
00190776416539MillenniumAvalign Technologies, Inc.HTE2026-02-16
03662663109468Mergence-A Preparation InstrumentationHighridge Medical, LLCHTE2026-02-11
00190376539003Intervertebral Disc Preparation InstrumentsALPHATEC SPINE, INC.HTE2026-02-10
M93072513543B0Life Instruments Life Instrument CorporationHTE2026-02-02
00840180545096General InstrumentsALPHATEC SPINE, INC.HTE2026-01-29
00840180545102General InstrumentsALPHATEC SPINE, INC.HTE2026-01-29
00840180545119General InstrumentsALPHATEC SPINE, INC.HTE2026-01-29
00840277133151Innomed, Inc.INNOMED, INC.HTE2026-01-16
00840180543313General InstrumentsALPHATEC SPINE, INC.HTE2025-12-31
00840180543320General InstrumentsALPHATEC SPINE, INC.HTE2025-12-31
00840180543337General InstrumentsALPHATEC SPINE, INC.HTE2025-12-31
00840180543344General InstrumentsALPHATEC SPINE, INC.HTE2025-12-31
00840180543351General InstrumentsALPHATEC SPINE, INC.HTE2025-12-31
00840180543368General InstrumentsALPHATEC SPINE, INC.HTE2025-12-31
03662663156905SOLITAIRE CERVICAL SPACER SYSTEMHighridge Medical, LLCHTE2025-12-29
00199150051687Medtronic Reusable InstrumentsMEDTRONIC SOFAMOR DANEK, INC.HTE2025-12-25
00199150051694Medtronic Reusable InstrumentsMEDTRONIC SOFAMOR DANEK, INC.HTE2025-12-25
00199150051700Medtronic Reusable InstrumentsMEDTRONIC SOFAMOR DANEK, INC.HTE2025-12-25
03662663272186Timberline Lateral Fusion SystemHighridge Medical, LLCHTE2025-12-18
03662663272193Timberline Lateral Fusion SystemHighridge Medical, LLCHTE2025-12-18
03662663272209Timberline Lateral Fusion SystemHighridge Medical, LLCHTE2025-12-18
03662663272216Timberline Lateral Fusion SystemHighridge Medical, LLCHTE2025-12-18
03662663272223Timberline Lateral Fusion SystemHighridge Medical, LLCHTE2025-12-18