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Cytophil, Inc

Last updated September 17, 2026

Information

Country: US
Address: 2485 Corporate Circle, Unit 2, East Troy, WI, 53120
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3007225376
DUNS Number: —

Catalogue (44)

Device	Model / Reference	Registries	Class	Status
Callisto Granules Beta-TCP Synthetic Bone Graft	02-100-03-VEX	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-005-01-MIL	FDA UDI	Class II	Unknown
Bank-It Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-005-01-PIB	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-010-02-MIL	FDA UDI	Class II	Unknown
Renú Voice	08-015-04-V04	FDA UDI	Class II	Active
RegenPerio Dental Beta-TCP	04-005-01-RGP	FDA UDI	Class II	Unknown
Bank-It Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-010-01-PIB	FDA UDI	Class II	Unknown
Trab-X SB Synthetic Bone Matrix	02-100-03-VTX	FDA UDI	Class II	Unknown
Osteo-i Synthetic Biphasic Dental Bone Graft Granules	03-005-01-SAS	FDA UDI	Class II	Unknown
RegenOsteo Orthopedic Beta-TCP	02-050-02-RGO	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Biphasic Dental Bone Graft Granules	03-010-01-MIL	FDA UDI	Class II	Unknown
Zavation ZV Graft Beta-TCP Synthetic Bone Graft	02-030-03-ZVG	FDA UDI	Class II	Active
Callisto Granules Beta-TCP Synthetic Bone Graft	02-050-02-VEX	FDA UDI	Class II	Unknown
RegenOsteo Orthopedic Beta-TCP	02-100-02-RGO	FDA UDI	Class II	Unknown
Osteo-i Synthetic Biphasic Dental Bone Graft Granules	03-010-01-SAS	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-010-01-MIL	FDA UDI	Class II	Unknown
Renú Gel	08-015-00-V04	FDA UDI	Class II	Active
Implant Logistics Synthetic Biphasic Dental Bone Graft Granules	03-030-02-MIL	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Biphasic Dental Bone Graft Granules	03-030-01-MIL	FDA UDI	Class II	Unknown
Bank-It Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-030-01-PIB	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Biphasic Dental Bone Graft Granules	03-005-02-MIL	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-005-02-MIL	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Biphasic Dental Bone Graft Granules	03-005-01-MIL	FDA UDI	Class II	Unknown
Renú Transoral Needle	12-000-00-ND1	FDA UDI	Class I	Active
Trab-X SB Synthetic Bone Matrix	02-050-02-VTX	FDA UDI	Class II	Unknown
Zavation ZV Graft Beta-TCP Synthetic Bone Graft	02-030-02-ZVG	FDA UDI	Class II	Active
Regento Regenerative Scaffold	02-100-03-VTX	FDA UDI	Class II	Unknown
Callisto Granules Beta-TCP Synthetic Bone Graft	02-050-03-VEX	FDA UDI	Class II	Unknown
Osteo-i Synthetic Biphasic Dental Bone Graft Granules	03-030-01-SAS	FDA UDI	Class II	Unknown
Implant Logistics Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-030-01-MIL	FDA UDI	Class II	Unknown
Trab-X SB Synthetic Bone Matrix	02-050-03-VTX	FDA UDI	Class II	Unknown
Bio \| TCP Beta-Tricalcium Phosphate Porous Granulate	04-010-01-BSB	FDA UDI	Class II	Active
Implant Logistics Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-030-02-MIL	FDA UDI	Class II	Unknown
Osteo-i Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-005-01-SAS	FDA UDI	Class II	Unknown
Osteo-i Synthetic Beta-Tricalcium Phosphate Dental Bone Graft Granules	04-010-01-SAS	FDA UDI	Class II	Unknown
Callisto Granules Beta-TCP Synthetic Bone Graft	02-200-02-VEX	FDA UDI	Class II	Unknown
Cytophil Tissue Marker	K072219	FDA 510(k)	Class II	Active
Vocalis And Vocalis Sm	K081816	FDA 510(k)	Class II	Active
Vocalis Gel	K081815	FDA 510(k)	Class II	Active
Calcium Hydroxylapatite Vocal Fold Implant	K121795	FDA 510(k)	Class II	Active
Periophil B-Tcp	K093871	FDA 510(k)	Class II	Active
Periophil Biphasic	K092788	FDA 510(k)	Class II	Active
Renu Gel	K150400	FDA 510(k)	Class II	Active
Osteophil Beta-Tcp	K102937	FDA 510(k)	Class II	Active

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jan 11, 2012	Z-1012-2012	—	terminated	Cytophil Corporation is recalling Periophil Biphasic Periophil Biphasic, Periobase Biphasic, and Periobone Biphasic because devices were inadvertently shipped after receiving an inadequate dose of radiation and this product may not be sterile.