FDA.reportPublic FDA data

Sklar®

Primary DI
10649111325779
Brand
Sklar®
Company
SKLAR CORPORATION
Model
41-1900
Device description
"HATFIELD CURETTE 3MM/5MM 11"""
Published
2019-02-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

Product Codes#

Code, Name table
CodeName
FZSCURETTE, SURGICAL, GENERAL USE

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FZSCurette, Surgical, General UseGeneral, Plastic Surgery1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10649111325779PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
1064911132577910649111325779

GMDN Terms#

Term, Definition table
TermDefinition
Bone curette, reusableA manual surgical instrument designed for cutting and excising bone tissue typically during an orthopaedic or a plastic surgery procedure. It is typically designed as a long, slender instrument with a handle at the proximal end and a concave, spoon-like tip which has a sharp edge, at the distal end, or it may be double-ended, and is used to facilitate the removal of the bone tissue without causing trauma to the surrounding muscles. It is typically made of high-grade stainless steel and is a common instrument of choice for the removal of the bone. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
006966006
Device count
1
Premarket exempt
true
Lot or batch
true
Serial number
true
No natural rubber latex
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10649111501326Sklar Instruments31-40742026-03-12
10649111294235Sklar®67-10202016-10-07
10649111183386Sklar40-73122019-09-24
10649111183560Sklar40-73132019-09-24
10649111183713Sklar40-73142019-09-24
10649111183881Sklar40-73152019-09-24
10649111183997Sklar40-73162019-09-24
10649111184260Sklar40-73172019-09-24
10649111184420Sklar40-73182019-09-24
10649111187896Sklar40-73402019-09-24
10649111087431Sklar Instruments96-01922025-11-12
10649111225369Sklar Instruments96-10922025-11-12
10649111226281Sklar Instruments96-10972025-11-12
10649111226458Sklar Instruments96-10982025-11-12
10649111226762Sklar Instruments96-11002025-11-12
10649111226984Sklar Instruments96-11022025-11-12
10649111227370Sklar Instruments96-11052025-11-12
10649111228056Sklar Instruments96-11102025-11-12
10649111228919Sklar Instruments96-11152025-11-12
10649111229817Sklar Instruments96-11202025-11-12

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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04052536215539tezoUlrich GmbH & Co. KGFZS2026-03-16
04052536215546tezoUlrich GmbH & Co. KGFZS2026-03-16
00810130207367MSIModern Surgical Instruments LLCFZS2026-03-12
00810130207374MSIModern Surgical Instruments LLCFZS2026-03-12
00810130207381MSIModern Surgical Instruments LLCFZS2026-03-12
00810130207398MSIModern Surgical Instruments LLCFZS2026-03-12
04052536017560tezoUlrich GmbH & Co. KGFZS2026-03-12
04052536017577tezoUlrich GmbH & Co. KGFZS2026-03-12
04052536017584tezoUlrich GmbH & Co. KGFZS2026-03-12
04052536017751tezoUlrich GmbH & Co. KGFZS2026-03-12
00810158219182PRINCETONPrinceton Medical Group, Inc.FZS2026-03-11
00810158219199PRINCETONPrinceton Medical Group, Inc.FZS2026-03-11
M93071015043SAT20Life InstrumentsLife Instrument CorporationFZS2026-03-06
M93071015044SAT20Life InstrumentsLife Instrument CorporationFZS2026-03-06
00810158218802PRINCETONPrinceton Medical Group, Inc.FZS2026-02-05
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M9307120160110Life Instruments Life Instrument CorporationFZS2026-02-02
00810158218598PRINCETONPrinceton Medical Group, Inc.FZS2026-01-16
00810158218604PRINCETONPrinceton Medical Group, Inc.FZS2026-01-16
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00810158218505PRINCETONPrinceton Medical Group, Inc.FZS2026-01-15
M930712150000Life InstrumentsLife Instrument CorporationFZS2026-01-09
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