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L H M Ent., Inc.

United StatesFDA 510(k) applicant, unverified

Devices
6

What L H M Ent., Inc. makes

L H M Ent., Inc. manufactures single-use, sterile medical irrigation kits, prefilled syringes (60cc), catheter care kits, and sterile bottles containing either water or 0.9% saline. Custom trays and kits are also produced for medical procedures. These products are designed for one-time use and are intended to maintain sterility and hygiene in clinical settings.

The company’s portfolio includes devices classified under FDA’s Class I and Class II categories, with some products requiring 510(k) clearance. These products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does L H M Ent., Inc. have in the registry?

The registry currently lists 6 devices for L H M Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list L H M Ent., Inc.'s devices?

Among its 6 most recently registered devices, L H M Ent., Inc. has devices listed in FDA 510(k) (6 devices).

What risk classes do L H M Ent., Inc.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for L H M Ent., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from L H M Ent., Inc. in the registry?

The most recently registered devices listed for L H M Ent., Inc. include IRRIGATION KIT, SINGLE-USE, STERILE, PREFILLED SYRINGE, 60CC, CATHETER CARE KITS and SINGLE-USE, STERILE 4OZ BOTTLE CONTAIN STER. WATER.

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