Atlas FDA

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

The Anspach Effort, Inc. — Predicate Candidate Screening

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

48 daysmedian FDA review time
243 days90th percentile
60clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K220485Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for WireThe Anspach Effort, Inc.2022-05-19910
K183545Anspach Helix Dissection ToolsThe Anspach Effort, Inc.2019-07-192110
K180063OCM-G1 AttachmentThe Anspach Effort, Inc.2018-03-27770
K133604ANSPACH EG1 HIGH SPEED SYSTEM, G1 ATTACHMENTSThe Anspach Effort, Inc.2014-01-104610
K131053ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTAThe Anspach Effort, Inc.2013-12-312590
K113476ANSPACH DISSECTION TOOLSThe Anspach Effort, Inc.2011-12-162435
K082637CRANIAL PERFORATORThe Anspach Effort, Inc.2008-12-221030
K080802EMAX 2 PLUS SYSTEM, MODEL EMAX 2 PLUS MOTOR, EMAX 2 CONSOLE>The Anspach Effort, Inc.2008-04-304023
K061297ANSPACH IMRI SAFE SURGICAL DRILL SYSTEMThe Anspach Effort, Inc.2007-01-262623
K063688SURGICAL IRRIGATION SYSTEM, IRRIGATION TUBEThe Anspach Effort, Inc.2007-01-16350
K052572ANSPACH KNOTLESS ANCHORThe Anspach Effort, Inc.2005-12-05774
K050628ANSPACH COUPLERThe Anspach Effort, Inc.2005-04-07270
K042783ANSPACH MINIMAL ACCESS SPINAL ATTACHMENT (MASA) SYSTEMThe Anspach Effort, Inc.2004-12-177224
K040186ANSPACH MRI SAFE SURGICAL DRILL SYSTEMThe Anspach Effort, Inc.2004-04-15792
K040076ANSPACH ADVANCED MICRO SAW ATTACHMENTSThe Anspach Effort, Inc.2004-03-15613
K030576ANSPACH IRRIGATION PUMP AND IRRIGATION PUMP IIThe Anspach Effort, Inc.2003-05-21861
K022907ANSPACH POWERED KERRISON SYSTEM (PKS)The Anspach Effort, Inc.2002-10-21480
K011444ANSPACH EMAX DRILL SYSTEMThe Anspach Effort, Inc.2001-08-088937
K002903ANSPACH ANGLED MICRONOSE ATTACHMENTThe Anspach Effort, Inc.2000-10-24361
K982991ANSPACH ACCESS CRANIAL PERFORATORThe Anspach Effort, Inc.1998-10-21550
K981688ANSPACH SUTURE ANCHORThe Anspach Effort, Inc.1998-07-13630
K974025ANSPACH SHIELDED ATTACHMENTThe Anspach Effort, Inc.1998-07-062565
K970530ANSPACH LUBRICATING SYSTEM IIThe Anspach Effort, Inc.1997-05-05821
K965069ANSPACH SUTURE ANCHORThe Anspach Effort, Inc.1997-02-12610
K965080ANSPACH MICROMAX SYSTEMThe Anspach Effort, Inc.1997-01-10228
K963686ANSPACH SUTURE ANCHOR (MODIFIED)The Anspach Effort, Inc.1996-11-25740
K960630ANSPAHC SPEED REDUCERThe Anspach Effort, Inc.1996-11-192842
K955084ASPACH 65,000 (MODIFICATION)The Anspach Effort, Inc.1996-01-17904
K945525ANSPACH SUTURE ANCHORThe Anspach Effort, Inc.1995-07-112430
K940535AUTO LUBE SYSTEMThe Anspach Effort, Inc.1994-03-21421
K921338ANSPACH MINI-PLATING SYSTEMThe Anspach Effort, Inc.1993-02-103290
K864314EFTEKHAR RECHANNELIZATION DRILL GUIDEThe Anspach Effort, Inc.1986-11-19160
K852592CO2 FOR ARTHROSCOPYThe Anspach Effort, Inc.1985-08-09510
K850389MULTIPLE OUTLET MANIFOLDThe Anspach Effort, Inc.1985-03-18450
K841296TUBE TENDERThe Anspach Effort, Inc.1984-06-11730
K831756ANSPACH 65,000The Anspach Effort, Inc.1983-09-291201
K830721WIRE TWISTERSThe Anspach Effort, Inc.1983-04-12350
K822065KAM SUCKERThe Anspach Effort, Inc.1982-08-16330
K820777MINI-MICRO ARTHROSCOPIC SCAPELThe Anspach Effort, Inc.1982-05-12501
K820289ANTHROSCOPIC SURGICAL TABLEThe Anspach Effort, Inc.1982-04-21770
K820776CANNUOATED TROCHARThe Anspach Effort, Inc.1982-04-15230
K820291KNEE SUPPORT FOR X-RAY & SURGERYThe Anspach Effort, Inc.1982-03-05300
K820290SELF RETAINING RETRACTOR FOR HAND SURGThe Anspach Effort, Inc.1982-03-05300
K820292EXTRACTOR IIIThe Anspach Effort, Inc.1982-03-02270
K820293BONE BIOPSY SETThe Anspach Effort, Inc.1982-03-01260
K820275ARTHROSCOPIC HARPOONThe Anspach Effort, Inc.1982-02-12100
K811996GATOR DRAPESThe Anspach Effort, Inc.1981-08-13290
K811717GATOR DRAPESThe Anspach Effort, Inc.1981-07-20320
K811115SUPERFLOW CANNULA FOR ARTHROS. SURGERYThe Anspach Effort, Inc.1981-07-01690
K811081MEDULLARY CANAL SCRAPERSThe Anspach Effort, Inc.1981-04-2980

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