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Data / Medical devices / Battery, Replacement, Rechargeable / United States

FDA-registered makers of Battery, Replacement, Rechargeable in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Battery, Replacement, Rechargeable (product code MOQ). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

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Device
Battery, Replacement, Rechargeable
Product code
MOQ
Country
United States

Makers of Battery, Replacement, Rechargeable in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Anybattery, IncRosemount, MN, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Aspen Surgical Products, Inc.Caledonia, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Cole InstrumentsAlpharetta, GA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Evergreen Orthopedic Research LabKirkland, WA, United StatesSpecification developer0000api.fda.gov
Insurgical, Inc.Austin, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Jabil Inc. (Monument)Monument, CO, United StatesContract manufacturer0000api.fda.gov
KLS-Martin L.P.Jacksonville, FL, United StatesSpecification developer0000api.fda.gov
Kerr CorporationOrange, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Linvatec CorporationLargo, FL, United StatesSpecification developer0000api.fda.gov
Microaire Surgical Instruments LLCCharlottesville, VA, United StatesManufacturer0000api.fda.gov
Retail Acquisition & Development Dba Interstate All BatteryUrbandale, IA, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Stryker Manufacturing KalamazooPortage, MI, United StatesContract manufacturer0000api.fda.gov
Stryker InstrumentsPortage, MI, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Synthes (USA) Products LLCWest Chester, PA, United StatesSpecification developer0000api.fda.gov
Techtronic Industries MedicalAnderson, SC, United StatesContract manufacturer0000api.fda.gov
The Anspach Effort, Inc.Palm Bch Gdns, FL, United StatesComplaint file establishment, Specification developer0020api.fda.gov
Totex Manufacturing IncTorrance, CA, United StatesContract manufacturer0000api.fda.gov
Triangle Manufacturing Co., Inc.Upper Saddle River, NJ, United StatesContract manufacturer0000api.fda.gov
Unipower Corp.Minnetonka, MN, United StatesManufacturer0000api.fda.gov
Zimmer Surgical, Inc.Dover, OH, United StatesManufacturer0000api.fda.gov

Updated November 2, 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.