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Trust & verification

Every claim carries its source, its date and its status.

AOR publishes nothing that cannot be traced to an official manufacturer or regulator document. This center collects the verification record behind the ecosystem so buyers, clinicians and partners can audit it directly.

Protocol

How content reaches this site

A four-step chain applies to specifications, regulatory status and clinical language alike.

  1. 01

    1. Official source only

    Data is taken from manufacturer documentation, certificates or regulator databases. Third-party summaries, resellers and marketing copy are not accepted as sources.

  2. 02

    2. Recorded, not paraphrased

    Scope is captured as the document states it. Where a record is a registration or listing rather than a clearance or approval, the page says exactly that.

  3. 03

    3. Source URL + verification date

    Each entry stores the source it came from and the date a human last confirmed it. Nothing is published without both fields.

  4. 04

    4. Status is visible

    Content is labelled verified or pending verification. Pending items stay visibly marked instead of being presented as fact or quietly removed.

Legend

What each status means

Verified. Confirmed against an official manufacturer or regulatory source, with a recorded source URL and verification date.
Confirmed against an official manufacturer or regulatory source, with a recorded source URL and verification date.
Manufacturer-provided. Supplied by the manufacturer and reproduced without modification. AOR has not independently tested this information.
Supplied by the manufacturer and reproduced without modification. AOR has not independently tested this information.
Pending verification. An official source has been requested and is not yet on file. Treat this information as provisional.
An official source has been requested and is not yet on file. Treat this information as provisional.
In review. A source has been submitted and is under internal review before publication.
A source has been submitted and is under internal review before publication.
Not applicable. No regulatory or manufacturer claim applies to this item.
No regulatory or manufacturer claim applies to this item.

Registry

Documents on file

6 official documents. Last registry review: 2026-08-07.

6 documents shown

  • RobotGymInternational / Internacional (ISO)Verified

    ISO 13485:2016 Quality Management System Certificate — UniGym All-in-One Home Gym System

    Certificate No. 381260197R0S · GB/T 42061-2022 / ISO 13485:2016 · Valid until 2029-07-30 · Shanghai POSI Certification Co., Ltd. (ANAB / IAF accredited) · Issued 2026-07-31

    Quality management system of JuShenZhiNeng Technology (Jiaxing) Co., Ltd registered for the production and sales of the UniGym All-in-One Home Gym System (export only). Attached sheet sites: production at JuShenZhiNeng Technology (Jiaxing) Co., Ltd; sales (export only) at Shanghai Rushen Robotics Co., Ltd. Initial issue 2026-07-31; valid until 2029-07-30, subject to surveillance audits. This is a quality management system registration — not a device approval or clearance.

    Last verified
    2026-08-07
    Content status
    Verified
  • AnovatorUnited States / Estados UnidosVerified

    FDA Establishment Registration & Device Listing — Body Composition Analyzer

    Product code PUH6 · 21 CFR 870.2770 · Class 2 (exempt) · U.S. Food and Drug Administration · Issued 2025-06-23

    Registration and listing record for Body Composition Analyzer (M, K, A, S and T series). Registered establishment: Wuhan Zhaike Network Technology Company, Limited (No. 3038208691). This is a registration and listing record only — not a 510(k) clearance, approval, or statement of clinical performance.

    Last verified
    2026-08-05
    Content status
    Verified
  • RobotGymEuropean Union / Unión EuropeaVerified

    EU-Type Examination Certificate (Notified Body 0980) — UniGym All-in-One System

    Reg. No. 3895-05-2025-250238 · Annex III, Module B, 2014/53/EU · Eurofins Electrical and Electronic Testing NA, Inc. · Issued 2025-05-13

    Results recorded as Conform for Art. 3.1(a) Safety, Art. 3.1(a) Health, Art. 3.1(b) EMC and Art. 3.2 Radio. Valid only in conjunction with the attached Annex.

    Last verified
    2026-08-05
    Content status
    Verified
  • RobotGymUnited States / Estados UnidosVerified

    FCC Grant of Equipment Authorization — UniGym All-in-One System

    FCC ID 2BOKL-C1001 · Part 15C · 2402.0–2480.0 MHz · Eurofins Electrical and Electronic Testing NA, Inc. (TCB) · Issued 2025-04-29

    Certification issued under the authority of the Federal Communications Commission. Equipment class: Digital Transmission System; 0.00201 W conducted output. The antenna must be installed with at least 20 cm separation from all persons. Grant is not transferable.

    Last verified
    2026-08-05
    Content status
    Verified
  • RobotGymEuropean Union / Unión EuropeaVerified

    CE / RED Verification of Conformity — UniGym All-in-One System

    No. STS2503061RE · Models C-1001-B, C-1001-P · Shenzhen STS Test Services Co., Ltd. · Issued 2025-04-16

    Tested against the standards used to show compliance with the essential requirements of Radio Equipment Directive (RED) 2014/53/EU. Manufacturer: Shanghai Rushen Robotics CO., LTD.

    Last verified
    2026-08-05
    Content status
    Verified
  • RobotGymUnited States / Estados UnidosVerified

    FCC Supplier's Declaration of Conformity (Part 15B) — UniGym All-in-One System

    No. STS2503061EF · Test report STS2503061E02 · Shenzhen STS Test Services Co., Ltd. · Issued 2025-03-31

    Compliance with FCC Part 15 Subpart B, measured according to ANSI C63.4-2014. Models C-1001-B and C-1001-P.

    Last verified
    2026-08-05
    Content status
    Verified

Registration or listing records are administrative and do not constitute clearance, approval or a claim of clinical performance. Availability and regulatory status vary by country.

Related

Where verification shows up

Need a document we have not published?

Request the specific certificate or technical file and we will confirm what exists, what is pending and what cannot be claimed.