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Snyder Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
16

What Snyder Laboratories, Inc. makes

Snyder Laboratories, Inc. manufactures surgical and medical drainage solutions, including irrigation trays, suction instruments, and specialized kits for procedures like catheterization, debridement, and hysterectomy. Their portfolio includes chest drainage systems, urinary drainage bags, vented wound kits, and connecting tubing for medical suction. Products are designed for use in operating rooms, wound care, and postoperative recovery settings.

The company’s devices are classified under FDA’s Class I and Class II categories, with some requiring 510(k) clearance. Products are listed in the FDA’s 510(k) database, reflecting their regulatory status in the United States. The manufacturer operates from its base in the US.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Snyder Laboratories, Inc. have in the registry?

The registry currently lists 16 devices for Snyder Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Snyder Laboratories, Inc.'s devices?

Among its 16 most recently registered devices, Snyder Laboratories, Inc. has devices listed in FDA 510(k) (16 devices).

What risk classes do Snyder Laboratories, Inc.'s devices fall under?

Among its 16 most recently registered devices, the classes recorded for Snyder Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Snyder Laboratories, Inc. in the registry?

The most recently registered devices listed for Snyder Laboratories, Inc. include GREENLINE IRRIGATION TRAYS, YANKAUER & POODLE SUCTION INSTRUMENTS, TRAY AND BAG, CATHETERIZATION and SNYDER HEMOVAC CHEST DRAINAGE SOLUTION.

Generated automatically from registry data and not verified by a human reviewer.