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Data / Medical devices / Blade, Scalpel / United States

FDA-registered makers of Blade, Scalpel in the United States: 52 establishments

52 establishments in the United States are registered with the FDA to make Blade, Scalpel (product code GES). 1 has a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 3, 2026.

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Device
Blade, Scalpel
Product code
GES
Country
United States

Makers of Blade, Scalpel in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Primrose Medical, Inc.East Walpole, MA, United StatesManufacturer1September 24, 1987000api.fda.gov
ARCH Medical Solutions - MemphisBartlett, TN, United StatesContract manufacturer0000api.fda.gov
ARCH Medical Solutions - MemphisLexington, TN, United StatesContract manufacturer0000api.fda.gov
Argon Medical Devices Inc.Athens, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Arthrex, Inc.Naples, FL, United StatesSpecification developer0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesManufacturer0000api.fda.gov
AccuTec, Inc.Verona, VA, United StatesManufacturer0000api.fda.gov
Apollo Renal Therapeutics, LLCOcala, FL, United StatesContract manufacturer0000api.fda.gov
Aspen Surgical Puerto Rico Corp.Colinas de San Agustin, PR, United StatesManufacturer0010api.fda.gov
Becton DickinsonFranklin Lakes, NJ, United StatesSpecification developer0030api.fda.gov
Biomet, Inc.Warsaw, IN, United StatesManufacturer0000api.fda.gov
Beaver-Visitec International, Inc.Waltham, MA, United StatesManufacturer, Specification developer0000api.fda.gov
Exelint International, Co.Redondo Beach, CA, United StatesManufacturer, Specification developer0000api.fda.gov
Fischer Surgical Inc.Imperial, MO, United StatesManufacturer0000api.fda.gov
Geotec, Inc.Warwick, RI, United StatesContract manufacturer0000api.fda.gov
HRS Instruments, LLCTucson, AZ, United StatesManufacturer0000api.fda.gov
Intelivation Technologies, LLCPlymouth Meeting, PA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
Integra LifeSciences Production CorporationMansfield, MA, United StatesSpecification developer0000api.fda.gov
Kapp Surgical, Inc.Cleveland, OH, United StatesManufacturer0000api.fda.gov
Katena Products, Inc.Parsippany, NJ, United StatesSpecification developer0000api.fda.gov
Katena Products, Inc.Randolph, NJ, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
KLS-Martin L.P.Jacksonville, FL, United StatesSpecification developer0000api.fda.gov
Mason Tayler Medical Products Corp.Buffalo, NY, United StatesSpecification developer0000api.fda.gov
MedenovateIrvine, CA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
MEDIPOINT Holdings, LLCMineola, NY, United StatesManufacturer0000api.fda.gov
Medtech LLCMillington, TN, United StatesContract manufacturer0000api.fda.gov
Merit Medical Systems, Inc.South Jordan, UT, United StatesSpecification developer0010api.fda.gov
Meta Dental Corp.Glendale, NY, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Medline ReNewalRedmond, OR, United StatesReprocessor0000api.fda.gov
Michael Todd Beauty, LPPort St Lucie, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Nano Surgical, IncDelray Beach, FL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Orchid UniqueBridgeport, MI, United StatesManufacturer0000api.fda.gov
Phoenix Instruments, Inc.Lisle, IL, United StatesContract manufacturer0000api.fda.gov
Propper MFG. Co., Inc.Long Island City, NY, United StatesManufacturer0000api.fda.gov
Planatome, LLCPhoenix, AZ, United StatesManufacturer, Remanufacturer0000api.fda.gov
Precision Medical Manufacturing LLCWheeling, IL, United StatesContract manufacturer, Manufacturer0000api.fda.gov
ProMed Concepts, LLCBrighton, TN, United StatesContract manufacturer0000api.fda.gov
Quality Tech Services, LLCBloomington, MN, United StatesContract manufacturer0000api.fda.gov
RC Consolidated Services, IncRancho Cucamonga, CA, United StatesSpecification developer0000api.fda.gov
Renovo, Inc.Bend, OR, United StatesReprocessor0000api.fda.gov
Ridge & Crest CompanyMonterey Park, CA, United StatesSpecification developer0000api.fda.gov
SIGN Fracture Care InternationalRichland, WA, United StatesSpecification developer0000api.fda.gov
Spectra Medical Devices, LLCWilmington, MA, United StatesSpecification developer0000api.fda.gov
Stryker EndoscopySan Jose, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Swissortho LLCProvidence, RI, United StatesSpecification developer0000api.fda.gov
Symmetry Medical Manufacturing IncClaypool, IN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Symmetry Medical Manufacturing Inc.Warsaw, IN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Teleflex LLC (NADC)Olive Branch, MS, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Vilex LLCMcminnville, TN, United StatesManufacturer0000api.fda.gov
Weco Manufacturing Group-HenriettaRochester, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Xodus Medical, Inc.New Kensington, PA, United StatesSpecification developer0000api.fda.gov

Updated November 3, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.