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Neoss, Ltd.

Last updated May 27, 2026

What Neoss, Ltd. makes

Neoss, Ltd. manufactures dental implant components, including permanent and temporary preformed suprastructures, two-piece screw endosteal implants, and single-use or reusable dental drill bits. Their portfolio also includes reusable instrument trays, surgical screwdrivers, and non-bioabsorbable pliable-polymer membranes for dental regeneration.

The company’s devices are classified under FDA regulations as Class I or Class II and are listed in the FDA’s Unique Device Identifier (UDI) database. Neoss, Ltd. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Address: —
Website: neoss.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 999-999-9999
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 216693627

Catalogue (530)

Page 8 of 11

Device	Model / Reference	Registries	Class	Status
Neoss Implant System	21207	FDA UDI	Class II	Active
Neoss Implant System	90243	FDA UDI	Class II	Active
Neoss Implant System	31304	FDA UDI	Class I	Active
Neoss Implant System	31366	FDA UDI	Class I	Active
Neoss Implant System	31307	FDA UDI	Class II	Active
Neoss Implant System	90144	FDA UDI	Class I	Active
Neoss Implant System	21227	FDA UDI	Class II	Active
Neoss Implant System	51139	FDA UDI	Class I	Active
Neoss Implant System	21424	FDA UDI	Class II	Active
Neoss Implant System	41190	FDA UDI	Class I	Unknown
Neoss Implant System	21178	FDA UDI	Class II	Active
Neoss Implant System	21194	FDA UDI	Class II	Active
Neoss Implant System	31368	FDA UDI	Class II	Active
Neoss Implant System	41182	EUDAMEDFDA UDI	Class II	Active
Neoss Implant System	31405	FDA UDI	Class II	Active
Neoss Implant System	31300	FDA UDI	Class I	Active
Neoss Implant System	31273	FDA UDI	Class II	Unknown
Neoss Implant System	31367	FDA UDI	Class II	Active
Neoss Implant System	21245	FDA UDI	Class II	Active
Neoss Implant System	31450	FDA UDI	Class I	Active
Neoss Implant System	31311	FDA UDI	Class II	Active
Neoss Implant System	31330	FDA UDI	Class II	Active
Neoss Implant System	31207	FDA UDI	Class II	Active
Neoss Implant System	51124	EUDAMEDFDA UDI	Class I	Active
Neoss Implant System	90112	FDA UDI	Class I	Active
Neoss Implant System	41180	EUDAMEDFDA UDI	Class II	Active
Neoss Implant System	31287	FDA UDI	Class II	Active
Neoss Implant System	31371	FDA UDI	Class II	Active
Neoss Implant System	64011	FDA UDI	Class II	Active
Neoss Implant System	51190	FDA UDI	Class I	Active
Neoss Implant System	51186	EUDAMEDFDA UDI	Class I	Active
Neoss Implant System	51155	EUDAMEDFDA UDI	Class I	Active
Neoss Implant System	41166	EUDAMEDFDA UDI	Class II	Active
Neoss Implant System	31365	FDA UDI	Class I	Active
Neoss Implant System	90213	FDA UDI	Class I	Active
Neoss Implant System	31206	FDA UDI	Class II	Active
Neoss Implant System	21228	FDA UDI	Class II	Active
Neoss Implant System	31266	FDA UDI	Class I	Active
Neoss Implant System	41154	EUDAMEDFDA UDI	Class II	Active
Neoss Implant System	31320	FDA UDI	Class II	Active
Neoss Implant System	51145	EUDAMEDFDA UDI	Class I	Active
Neoss Implant System	31351	FDA UDI	Class I	Active
Neoss Implant System	31260	FDA UDI	Class II	Active
Neoss Implant System	90241	FDA UDI	Class II	Active
Neoss Implant System	21426	FDA UDI	Class II	Active
Neoss Implant System	31340	FDA UDI	Class II	Active
Neoss Implant System	41238	EUDAMEDFDA UDI	Class II	Active
Neoss Implant System	31185	FDA UDI	Class I	Active
Neoss Implant System	31375	FDA UDI	Class II	Active
Neoss Implant System	Dolder Bar Ti	FDA UDI	Class II	Active

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