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Data / Medical devices / Laparoscopic Accessories, Gynecologic / United States

FDA-registered makers of Laparoscopic Accessories, Gynecologic in the United States: 20 establishments

20 establishments in the United States are registered with the FDA to make Laparoscopic Accessories, Gynecologic (product code NWV). 0 have 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
Laparoscopic Accessories, Gynecologic
Product code
NWV
Country
United States

Makers of Laparoscopic Accessories, Gynecologic in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Applied Medical Resources Corp.Rsm, CA, United StatesComplaint file establishment, Manufacturer0020api.fda.gov
Applied Medical Distribution CenterIrvine, CA, United StatesManufacturer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer0000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer0010api.fda.gov
Cook IncorporatedSpencer, IN, United StatesManufacturer0000api.fda.gov
Elmed, Inc.Glendale Heights, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Flexbar Machine Corp.Islandia, NY, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Integra LifeSciences Production CorporationMansfield, MA, United StatesSpecification developer0000api.fda.gov
Jackson Medical GroupMarietta, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
JosNoe Medical IncNixa, MO, United StatesSpecification developer0010api.fda.gov
Lapovations, LLCFayetteville, AR, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Mahe Medical UsaLaramie, WY, United StatesComplaint file establishment, Specification developer0000api.fda.gov
National Advanced Endoscopy Devices, Inc.Canoga Park, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Novaprobe Inc.Lansdale, PA, United StatesManufacturer, Remanufacturer, Specification developer0000api.fda.gov
Pristech Products, Inc.San Antonio, TX, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Stryker Sustainability SolutionsTempe, AZ, United StatesSpecification developer0000api.fda.gov
Stryker Sustainability Solutions LakelandLakeland, FL, United StatesReprocessor0000api.fda.gov
Tech Medical Services, Inc.Nixa, MO, United StatesRepackager or relabeler, Specification developer0000api.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

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.