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Think Surgical Inc.

Last updated September 17, 2026

Information

Country: US
Address: 47201 Lakeview Blvd, Fremont, CA, 94538
Website: —
LinkedIn: —
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Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3000719653
DUNS Number: —

Catalogue (99)

Page 1 of 2

Device	Model / Reference	Registries	Class	Status
TMINI® Guide Block Kit for Maxx Ortho Freedom® Total & Titan Knee (10ea)	109900-J	FDA UDI	Class II	Active
Tracking Array Bracket	109091	FDA UDI	Class II	Active
Tsolution One Surgical System	105716	FDA UDI	Class II	Active
Tsolution One Surgical System	103593	FDA UDI	Class II	Active
Tsolution One Surgical System	108200	FDA UDI	Class II	Active
Tsolution One Surgical System	107667	FDA UDI	Class II	Active
Tsolution One Surgical System	105934	FDA UDI	Class II	Active
Tsolution One Surgical System	103306	FDA UDI	Class II	Active
TMINI® Guide Block Kit for Maxx Ortho Freedom® Total & Titan Knee	109982	FDA UDI	Class II	Active
Tsolution One Surgical System	100086	FDA UDI	Class II	Active
TMINI® Guide Block Kit for Medacta® Knee System (10ea)	109900-E	FDA UDI	Class II	Active
TMINI® Guide Block Kit for LINK® LinkSymphoKnee System	109975	FDA UDI	Class II	Active
TMINI® Guide Block Kit for United® U2™ Knee (10ea)	109900-D	FDA UDI	Class II	Active
TMINI® Guide Block Kit for Zimmer Biomet: Posterior Referencing Persona® (10ea)	109900-K	FDA UDI	Class II	Active
Tsolution One Surgical System	107645	FDA UDI	Class II	Active
TMINI™ Guide Block Kit for BKS® and BKS TriMax® Knee System	109481	FDA UDI	Class II	Active
Tsolution One Surgical System	106298-04	FDA UDI	Class II	Active
Tsolution One Surgical System	107650	FDA UDI	Class II	Active
Tibia Tracking Array	109004	FDA UDI	Class II	Active
Tsolution One Surgical System	103305	FDA UDI	Class II	Active
Tsolution One Surgical System	106382	FDA UDI	Class II	Active
Tsolution One Surgical System	107649	FDA UDI	Class II	Active
Digitizer	109005	FDA UDI	Class II	Active
TMINI® Guide Block Kit for Zimmer Biomet: Posterior Referencing Persona® Knee	109992	FDA UDI	Class II	Active
TMINI™ Tray	109426	FDA UDI	Class II	Active
TMINI® Guide Block Kit for LINK® LinkSymphoKnee System (10ea)	109900-G	FDA UDI	Class II	Active
Tsolution One Surgical System	100573	FDA UDI	Class II	Active
TMINI® Guide Block Kit for Zimmer Biomet: Anterior Referencing Persona® (10ea)	109900-L	FDA UDI	Class II	Active
THINK Case Manager	109939	FDA UDI	Class II	Active
Tsolution One Surgical System	106219	FDA UDI	Class II	Active
Tsolution One Surgical System	107666	FDA UDI	Class II	Active
Universal Cut Block	106927	FDA UDI	Class II	Active
CT Motion Rod, 42 inch	103725	FDA UDI	Class II	Active
Tsolution One Surgical System	103636	FDA UDI	Class II	Active
Tsolution One Surgical System	103414	FDA UDI	Class II	Active
Tsolution One Surgical System	105653	FDA UDI	Class II	Active
CT Motion Rod, 54 inch	103449	FDA UDI	Class II	Active
TMINI™ Guide Block Kit for Enovis™ EMPOWR Knee System®	109421	FDA UDI	Class II	Active
TMINI® Guide Block Kit for b-ONE MOBIO® Total Knee System (10ea)	109900-F	FDA UDI	Class II	Active
Square Driver	109126	FDA UDI	Class II	Active
Tsolution One Surgical System	101884	FDA UDI	Class II	Active
TMINI® Guide Block Kit for Medacta® Knee System	109973	FDA UDI	Class II	Active
Tsolution One Surgical System	102709	FDA UDI	Class II	Active
Angel Wing	109079	FDA UDI	Class II	Active
Tsolution One Surgical System	104948	FDA UDI	Class II	Active
Tsolution One Surgical System	102862-NS	FDA UDI	Class II	Active
TMINI™ Knee Surgery Kit	109425	FDA UDI	Class II	Active
TMINI™ Navigation Console	108757	FDA UDI	Class II	Active
Tsolution One Surgical System	102940	FDA UDI	Class II	Active
TMINI™ Guide Block Kit for Klassic® Knee System	109482	FDA UDI	Class II	Active

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FDA Recalls (2)

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
Feb 12, 2024	Z-1318-2024	—	open, classified	There is a galling effect (cold-weld) caused by friction between the array fixation pins and the TMINI array guide holes due to insufficient clearance between the outer diameter of the fixation pins and the inner diameter of the TMINI array guide holes. As a result, the array guide has the possibility of binding to the array fixation pins during drilling.
Mar 30, 2018	Z-2605-2018	—	terminated	There is a potential for the cutter head to detach from the cutter shaft.