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.
- 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.
- 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.
- 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.
- 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.
- Source URL
- posicert.com · cx.cnca.cn
- 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.
- Source URL
- accessdata.fda.gov
- 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.
- Source URL
- Notified Body 0980
- 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.
- Source URL
- Telecommunication Certification Body
- 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.
- Source URL
- Manufacturer-issued certificate
- 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.
- Source URL
- Manufacturer-issued declaration
- 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.
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.
