Atlas FDA

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

Surgical Instruments Service and Savings, Inc. · Predicate Candidate Screening

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

294 daysmedian FDA review time
375 days90th percentile
8clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K124033MEDISISS REPROCESSED ULTRASONIC INSTRUMENTSSurgical Instruments Service and Savings, Inc.2014-01-073750
K031869SISS INC. (D.B.A. MEDISISS) REPROCESSED ELECTROSURGICAL INSTSurgical Instruments Service and Savings, Inc.2003-12-241900
K030179MEDISISS PHACOEMULSIFICATION TIPS/NEEDLESSurgical Instruments Service and Savings, Inc.2003-01-2471
K024011SISS REPROCESSED HOT BIOPSY FORCEPS, LAPAROSCOPIC, ENDOSCOPISurgical Instruments Service and Savings, Inc.2002-12-19150
K012644REPROCESSED TROCARS AND CANNULASSurgical Instruments Service and Savings, Inc.2002-07-293501
K012669REPROCESSED ELECTROSURGICAL ELECTRODESSurgical Instruments Service and Savings, Inc.2002-06-273185
K012667REPROCESSED ARTHROSCOPIC SHAPERSSurgical Instruments Service and Savings, Inc.2002-06-032942
K012658REPROCESSED COMPRESSION LIMB SLEEVESSurgical Instruments Service and Savings, Inc.2002-05-142741

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