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Biorep Technologies, INC.

15804 Nw 57th Ave, Miami Lakes, FL 33014

ACTIVELAST SEEN IN FEDERAL DATA AUG 2026 · 3 SOURCES

Operating signal within 12 months from two or more independent sources.

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Homepage of Biorep Technologies, INC.
Their homepage, crawled JUL 2026

What they make

Surgical and Medical Instrument Manufacturing339112

Biorep Technologies provides contract design, manufacturing, prototyping, and assembly services for medical devices. The company serves medical device developers across various therapeutic areas and operates as a CDMO (contract development and manufacturing organization). Biorep is ISO 13485 certified and FDA-registered.

SUMMARIZED FROM THE COMPANY’S OWN WEBSITE

Products

Made or handled here · 3
Clamp, Vascular · Instruments, Surgical, Cardiovascular · Syringe, Irrigating (Non Dental)
Where these came from
3 from FDA device registration · Federal registry
FDA device establishment 3005593675, product code DXC; proprietary names: MI DeTACH Aortic Cross Clamp Delivery Device, MI DeTACH Aortic Cross Clamp Head Small, MI DeTACH Aortic Cr

CERTIFICATIONS — LISTED ON THE COMPANY’S WEBSITE

  • FDA registered
  • ISO 13485

Read from this company’s own website on August 9, 2026. Nobody at the facility has confirmed it here, and FactoryRegistry has not verified these — unlike operating status, which comes from independent public records. A certificate can lapse without the website changing, so ask the facility for current ones.

Where it is

Location not verified — this address could not be matched to Census TIGER, so the facility is not placed on the map.

ON GOOGLE MAPS
STREET VIEW

Other plants nearby

No other listed facility within 40 km shares this one’s four-digit industry code, or this record has no coordinates to measure from.

Also at this address

No other federal record shares this street address.

WHERE THIS RECORD COMES FROM — 3 FEDERAL SOURCES, 7 FIELDS

Every fact on this page traces to a public federal filing. The table below names which register holds this facility, whether that register proves the plant operates or only that it exists, and when each of them last saw it.

SourceEvidenceFirst seenLast seen
FDA DEVICESOPERATINGAUG 2026AUG 2026
COMPANY SITEOPERATINGJUL 2026AUG 2026
SAM GOVOPERATINGAUG 2025AUG 2025
FIELD BY FIELD — WHICH SOURCE SUPPLIED WHAT
FIELDSOURCESIGNAL
ADDRESS LINE1SAM GOVAUG 2025
CAGE CODESAM GOVAUG 2025
CITYSAM GOVAUG 2025
NAMESAM GOVAUG 2025
REGISTRATION EXPIRATIONSAM GOVAUG 2025
STATESAM GOVAUG 2025
WEBSITESAM GOVAUG 2025

Status is computed from independent sources; nothing here is self-reported unless marked Claimed.

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