Atlas FDA

Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account

Computer Motion, Inc. — Predicate Candidate Screening

26 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.

60 daysmedian FDA review time
238 days90th percentile
26clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K031956MODIFICATION TO HERMES O.R. CONTROL CENTERComputer Motion, Inc.2003-07-17220
K031720MODIFICATION TO HERMES O.R. CONTROL CENTERComputer Motion, Inc.2003-07-11380
K031382MODIFICATION TO HERMES O.R. CONTROL CENTERComputer Motion, Inc.2003-06-30600
K030578BIPOLAR GRASPER AND BIPOLAR SCISSORS FOR THE ZEUS MICROWRISTComputer Motion, Inc.2003-06-241200
K030718SCB COMPUTER MOTION INTERFACE CONTROLLERComputer Motion, Inc.2003-06-05900
K030240MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.2003-02-21290
K024294MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.2003-01-08150
K023095HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.2002-11-15580
K022897MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.2002-10-11380
K021152ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEM AND ACCESSORIESComputer Motion, Inc.2002-09-241670
K013551ZEUS MICROWRIST ROBOTIC SURGICAL SYSTEMComputer Motion, Inc.2002-03-281550
K013804SOCRATES ROBOTIC TELEMONITORING SYSTEMComputer Motion, Inc.2001-12-10250
K003431ZEUS ROBOTIC SURGICAL SYSTEMComputer Motion, Inc.2001-10-053360
K003661SOCRATES ROBOTIC TELEMONITORING SYSTEMComputer Motion, Inc.2001-10-053110
K003222MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.2000-11-03180
K003217HERMES PORT EXPANDERComputer Motion, Inc.2000-11-03210
K991444HERMES CONTROL CENTER, WITH CONTROL OF THE AESOP 3000HR (HERComputer Motion, Inc.1999-06-25600
K991734MODIFICATION OF: HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.1999-06-09190
K991635MODIFICATION TO HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.1999-05-27150
K990691HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.1999-03-23200
K980787HERMES OPERATING ROOM CONTROL CENTER WITH THE WOM 20L INSUFFComputer Motion, Inc.1998-07-131330
K973700HERMES OPERATING ROOM CONTROL CENTERComputer Motion, Inc.1998-02-241510
K972699AESOP 3000 SYSTEM AND ACCESSORIESComputer Motion, Inc.1997-12-191540
K963126AESOP SYSTEM AND ACCESSORIESComputer Motion, Inc.1997-04-072380
K960655AESOP SYSTEM AND ACCESSORIESComputer Motion, Inc.1996-05-03780
K931783AESOP (AUTOMATED ENDOSCOPIC SYSTEM FOR OPTIMAL POSComputer Motion, Inc.1993-11-222270

Methodology

Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.

Prepared with Atlas

Predicate research, review-time statistics and recall monitoring for 510(k) teams — atlasbyauro.com/fda