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Johnson & Johnson Professionals, Inc.

Country not established

Devices
206

What Johnson & Johnson Professionals, Inc. makes

Johnson & Johnson Professionals, Inc. manufactures orthopedic implants including unicompartmental and total knee systems (e.g., P.F.C. and Darwin TC3), hip femoral prostheses with porous coatings, and absorbable fixation pins (e.g., PDS). Their portfolio also includes cardiovascular devices like hollow fiber oxygenators (e.g., Maxima) and dental materials such as porcelain veneer cementation systems, light-curing composites, and casting tapes. Surgical accessories like dispersible alloy implants and dental activators are also part of their offerings.

The company’s devices are regulated under FDA classifications spanning Class I, II, III, and Unclassified (U), with many cleared via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry, reflecting their compliance with U.S. medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue206

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  • Ti-Frame Ref K934860

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Carefree * Panty Shields-Reg/Deor Ref K832382

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Stayfree* Deodorant Maxi-Pads Ref K834302

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Codman Intracranial Bolt Ref K974088

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Emergency Department Laceration Kit- Ref K802557

    Active Regimes: 510(k) Registry: 510(k) Class:I

  • Bandage, Triangular No. 8068 Ref K760250

    Active Regimes: 510(k) Registry: 510(k) Class:I

Showing 201-206 of 206