Atlas FDA

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

Interpro Intl., Inc. — Predicate Candidate Screening

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

77 daysmedian FDA review time
142 days90th percentile
11clearances measured
K-numberDeviceApplicantDecidedReview daysRecalls (K-match)
K890968VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)Interpro Intl., Inc.1989-07-311540
K890891LATEX EXAMINATION GLOVES (MFG. NINGBO MEDICAL)Interpro Intl., Inc.1989-07-141420
K891642PATIENT EXAMINATION GLOVES (LATEX)Interpro Intl., Inc.1989-07-141190
K891440PATIENT EXAMINATION GLOVES (LATEX)Interpro Intl., Inc.1989-05-31770
K891438PATIENT EXAMINATION GLOVES (LATEX)Interpro Intl., Inc.1989-05-31770
K881374SURGEONS GLOVESInterpro Intl., Inc.1988-08-051260
K874067GUAZE SPONGESInterpro Intl., Inc.1987-12-14700
K874766INTERPRO INT'L, INC. ISOLATION GOWNInterpro Intl., Inc.1987-12-10210
K874064SHOE COVERSInterpro Intl., Inc.1987-11-04300
K874065LAPAROTOMY SPONGESInterpro Intl., Inc.1987-11-04300
K874066SURGICAL CAPSInterpro Intl., Inc.1987-11-04300

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